Alliance Medical Corp.
Phoenix, AZ, US
Alliance Medical Corp. appears in FDA device records in Phoenix, AZ. FDA records list 47 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 47
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 47 510(k) clearances for Alliance Medical Corp. between 1994 and 2007. The busiest year on record is 2005, with 11. The most recent is 2007, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 1 |
| 1996 | 1 |
| 1999 | 1 |
| 2001 | 10 |
| 2002 | 5 |
| 2003 | 10 |
| 2004 | 1 |
| 2005 | 11 |
| 2006 | 6 |
| 2007 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K060648 | REPROCESSED PHACOEMULSIFICATION TIPS | NKX | Substantially Equivalent | |
| K061045 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | NLH | Substantially Equivalent | |
| K051438 | VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM) | JOW | Substantially Equivalent | |
| K060049 | REPROCESSED COMPRESSION SLEEVES | JOW | Substantially Equivalent | |
| K060091 | ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES | JOW | Substantially Equivalent | |
| K053316 | REPROCESSED COMPRESSION SLEEVES | JOW | Substantially Equivalent | |
| K052918 | REPROCESSED EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K052603 | REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS | NLH | Substantially Equivalent | |
| K052414 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K050518 | REPROCESSED PHACOEMUISIFICATION TIPS | NKX | Substantially Equivalent | |
| K052064 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K052062 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K052065 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K051554 | ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K043358 | REPROCESSED ULTRASONIC SCALPELS | NLQ | Substantially Equivalent | |
| K043392 | REPROCESSED ELECTROPHYSIOLOGY CATHETERS | NLH | Substantially Equivalent | |
| K043393 | REPROCESSED EP TECHNOLOGIES ELECTROPHYSIOLOGY CATHETERS | NLH | Substantially Equivalent | |
| K033436 | REPROCESSED DIAGNOSTIC ULTRASOUND CATHETER | OWQ | Substantially Equivalent | |
| K041978 | REPROCESSED DIAMOND BURS | NLN | Substantially Equivalent | |
| K030279 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K030187 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K030109 | ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K032058 | MODIFICATION TO REPROCESSED SYNTHES EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K030026 | REPROCESSED ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K024087 | REPROCESSED COMPRESSION SLEEVES | JOW | Substantially Equivalent | |
| K024074 | REPROCESSED COMPRESSION SLEEVES | JOW | Substantially Equivalent | |
| K024015 | REPROCESSED ENDOSCOPIC TROCARS AND CANNULAS | NLM | Substantially Equivalent | |
| K021654 | REPROCESSED COMPRESSION SLEEVE | JOW | Substantially Equivalent | |
| K023714 | REPROCESSED EXTERNAL FIXATION DEVICE | KTT | Substantially Equivalent | |
| K012708 | ELECTROPHYSIOLOGY CATHETER | NLH | Substantially Equivalent | |
| K012648 | REPROCESSED HOWMEDICA EXTERNAL FIXATION DEVICES | KTT | Substantially Equivalent | |
| K012645 | REPROCESSED EBI EXTERNAL FIXATION DEVICES | KTW | Substantially Equivalent | |
| K012634 | REPROCESSED EXTERNAL FIXATION DEVICE | KTW | Substantially Equivalent | |
| K012623 | REPROCESSED EXTERNAL FIXATION DEVICE | KTT | Substantially Equivalent | |
| K012631 | REPROCESSED SOFT TISSUE ABLATORS | GEI | Substantially Equivalent | |
| K011192 | COMPRESSIBLE LIMB SLEEVE | JOW | Substantially Equivalent | |
| K012630 | REPROCESSED LINVATEC ARTHROSCOPIC BURS | HRX | Substantially Equivalent | |
| K012652 | REPROCESSED DYONICS ARTHROSCOPIC BURS | HRX | Substantially Equivalent | |
| K012635 | REPROCESSED STRYKER ARTHROSCOPIC SHAVERS | HRX | Substantially Equivalent | |
| K012613 | REPROCSSED LINVATEC SHAVERS | HRX | Substantially Equivalent | |
| K012611 | REPROCESSED DYONICS ARTHROSCOPIC SHAVERS | HRX | Substantially Equivalent | |
| K012605 | REPROCESSED ATHROSCOPICS BURS | HRX | Substantially Equivalent | |
| K012603 | REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS | NUJ | Substantially Equivalent | |
| K012625 | REPROCESSED UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS | GEI | Substantially Equivalent | |
| K990198 | AMIB7 | IYO | Substantially Equivalent | |
| K951976 | ECHO. AKHO | IYO | Substantially Equivalent | |
| K931091 | DISPOSABLE AMA STERILE DRAPE SHEET, CAT. NO. 5252 | KKX | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KTWAppliance, Fixation, Nail/Blade/Plate Combination, Single Component
- HRXArthroscope
- NLHCatheter, Recording, Electrode, Reprocessed
- KKXDrape, Surgical, Antimicrobial
- NLNDrills, Burrs, Trephines And Accessories (Simple Powered), Reprocessed
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- NUJElectrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
- NLMLaparoscope, General & Plastic Surgery, Reprocessed
- NKXNeedle, Phacoemulsification, Reprocessed
- OWQReprocessed Intravascular Ultrasound Catheter
- NLQSingle-Use Reprocessed Ultrasonic Surgical Instruments
- JOWSleeve, Limb, Compressible
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain