Intl. Medical, Inc.
Mchenry, IL, US
Intl. Medical, Inc. appears in FDA device records in Mchenry, IL. FDA records list 17 510(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
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Intl. Medical, Inc. between 1979 and 1997. The busiest year on record is 1994, with 4. The most recent is 1997, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1979 | 1 |
| 1984 | 2 |
| 1985 | 1 |
| 1990 | 2 |
| 1991 | 2 |
| 1992 | 2 |
| 1993 | 2 |
| 1994 | 4 |
| 1997 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K970507 | PEAK FLOW METER | BZH | Substantially Equivalent | |
| K943078 | HOT BIOPSY FORCEPS | KGE | Substantially Equivalent | |
| K940370 | AMERICAN CATHETER E.R.C.P. CANNULA | FGE | Substantially Equivalent | |
| K940335 | AMERICAN CATHETER POLY-SNARE | FDI | Substantially Equivalent | |
| K942068 | AMERICAN CATHETER SPHINCTEROTOME | KNS | Substantially Equivalent | |
| K930410 | DURHAM; LUER LOCK EXTENSION SET | FPA | Substantially Equivalent | |
| K930406 | DURHAM; MIN BORE LUER LOCK EXTENSION SET | FPA | Substantially Equivalent | |
| K923200 | AMCATH DISPOSABLE CYTOLOGY BRUSH | FDX | Substantially Equivalent | |
| K915142 | AMCATH DISPOSABLE BIOPSY FORCEPS | FCF | Substantially Equivalent | |
| K912927 | AMCATH DISPOSABLE TROCAR AND TROCAR SLEEVE | GCJ | Substantially Equivalent | |
| K912605 | AMCATH DISPOSABLE MICRO SCISSORS | GCJ | Substantially Equivalent | |
| K902555 | AMCATH COAGULATION PROBE | HFG | Substantially Equivalent | |
| K900988 | AMCATH SUCTION-IRRIGATION TUBE | HET | Substantially Equivalent | |
| K844744 | CARDIO IV/GXT STRESS TESTING SYSTEM | DPS | Substantially Equivalent | |
| K842339 | COMPUSTRESS STRESS TESTING SYS | DQK | Substantially Equivalent | |
| K833728 | CARDIAC WALL MOTION DEVICE | DSB | Substantially Equivalent | |
| K790476 | QUICKSCAN HOLTER II | DSH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HFGCoagulator, Laparoscopic, Unipolar (And Accessories)
- DQKComputer, Diagnostic, Programmable
- DPSElectrocardiograph
- FDXEndoscopic Cytology Brush
- KGEForceps, Biopsy, Electric
- FCFInstrument, Biopsy, Mechanical, Gastrointestinal
- GCJLaparoscope, General & Plastic Surgery
- HETLaparoscope, Gynecologic (And Accessories)
- BZHMeter, Peak Flow, Spirometry
- DSBPlethysmograph, Impedance
- DSHRecorder, Magnetic Tape, Medical
- FPASet, Administration, Intravascular
- FDISnare, Flexible
- FGEStents, Drains And Dilators For The Biliary Ducts
- KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain