Technicare Corp.
Mchenry, IL, US
Technicare Corp. appears in FDA device records in Mchenry, IL. FDA records list 32 510(k) clearances between and , 15 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
- 32
- PMA records
- 15
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 32 510(k) clearances for Technicare Corp. between 1980 and 1985. The busiest year on record is 1982, with 10. The most recent is 1985, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 3 |
| 1981 | 5 |
| 1982 | 10 |
| 1983 | 3 |
| 1984 | 7 |
| 1985 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K854340 | TECHNICARE 720 HPS CT SCANNER | JAK | Substantially Equivalent | |
| K852089 | SATURN NUCLEAR MEDICINE COMPUTER SYSTEM | IYX | Substantially Equivalent | |
| K844293 | AUTO DII MULTI FREQUENCY | IYN | Substantially Equivalent | |
| K844247 | ULTRASONIC SCANNER CALIBRATION & TEST PHANTOMS | GXX | Substantially Equivalent | |
| K843716 | NUCLEAR 700 MEDICINE MECHANICAL POSIT- | IYX | Substantially Equivalent | |
| K842777 | AUTOFOCUS DUAL ELEMENT PROBE | IYO | Substantially Equivalent | |
| K841817 | TECHNICARE 248 SL & 260SL | IYO | Substantially Equivalent | |
| K840860 | CENTAURI CT SCANNER | JAK | Substantially Equivalent | |
| K840540 | TECHNICARE MODEL 330 | IYO | Substantially Equivalent | |
| K834486 | TECHNICARE 280 | IYO | Substantially Equivalent | |
| K840390 | TECHNICARE MODEL 1047 | JAA | Substantially Equivalent | |
| K837499 | AUTOSECTOR | Substantially Equivalent | ||
| K837430 | AUTO D OPTION | Substantially Equivalent | ||
| K837046 | AUTOFOCUS PROBE FOR USE WITH ULTRASOUND AUTOSECTOR SYSTEM | Substantially Equivalent | ||
| K827644 | DELTASCAN HPS CT SCANNER | Substantially Equivalent | ||
| K827652 | TECHNICARE ULTRASOUND AUTO SECTOR B-SCAN ARM OPTION | Substantially Equivalent | ||
| K827610 | ULTRASOUND AUTO SECTOR CARDIAC MODULE | Substantially Equivalent | ||
| K827571 | MOBILE DIGITAL RECEPTOR | Substantially Equivalent | ||
| K827501 | MODEL 580 DIGITAL RADIOGRAPHY SYSTEM | Substantially Equivalent | ||
| K827378 | DIAGNOSTIC X-RAY HV GENERATOR | Substantially Equivalent | ||
| K827122 | DELTA PLAN II RADIATION THERAPY PLANNING SYSTEM | Substantially Equivalent | ||
| K820310 | DELTA PLAN II RADIATION THERAPY PLAN | IYE | Substantially Equivalent | |
| K827036 | AUTO SECTOR MCU | Substantially Equivalent | ||
| K813596 | AUTO SECTOR MCU | IYO | Substantially Equivalent | |
| K813196 | IMAGE ANALYSIS CENTER | JAK | Substantially Equivalent | |
| K813073 | OMEGA 500 RECTANGULAR FIELD CAMERA W/SC | IYX | Substantially Equivalent | |
| K812743 | FETAL VITABILITY TM MODE | IYO | Substantially Equivalent | |
| K812410 | DELTASCAN 2060 CT SCANNER | JAK | Substantially Equivalent | |
| K811931 | NEEDLE GUIDE ATTACHMENT | IYO | Substantially Equivalent | |
| K801948 | DIGITAL SUBTRACTION RADIOGRAPHY SYSTEM | JAA | Substantially Equivalent | |
| K801056 | EDP 1200 ULTRASONIC B-SCANNER | IYO | Substantially Equivalent | |
| K800892 | NUCLEAR STRESS TABLE (NST-1) | ISD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- IYEAccelerator, Linear, Medical
- GXXBlock, Test, Ultrasonic Scanner Calibration
- IYXCamera, Scintillation (Gamma)
- ISDExerciser, Measuring
- IYNSystem, Imaging, Pulsed Doppler, Ultrasonic
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- LNHSystem, Nuclear Magnetic Resonance Imaging
- JAASystem, X-Ray, Fluoroscopic, Image-Intensified
- JAKSystem, X-Ray, Tomography, Computed
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