Med-Tek Corp.
Mchenry, IL, US
Med-Tek Corp. appears in FDA device records in Mchenry, IL. FDA records list 16 510(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
- 16
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 16 510(k) clearances for Med-Tek Corp. between 1978 and 1990. The busiest year on record is 1990, with 10. The most recent is 1990, with 10.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1980 | 2 |
| 1981 | 1 |
| 1989 | 2 |
| 1990 | 10 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K903234 | F-19 TOTAL HIP PROSTHESIS | JDI | Substantially Equivalent | |
| K901687 | F-24 FEMORAL HIP PROSTHESIS | LWJ | Substantially Equivalent | |
| K901451 | F-20 CEMENTED METAL-BACKED ACETABULAR CUP | JDI | Substantially Equivalent for Some Indications | |
| K900428 | ANESTHESIA BREATHING CIRCUITS | CAI | Substantially Equivalent | |
| K901626 | H.N. METAL BACKED ACETABULAR CUP, NONCEMENTED | KWA | Substantially Equivalent | |
| K901594 | H.N. TOTAL HIP PROSTHESIS | LWJ | Substantially Equivalent | |
| K901480 | F-20 TOTAL HIP PROSTHESIS | JDI | Substantially Equivalent | |
| K901273 | L.M.S. SELF-DETACHABLE BROACH WITH STOP | HTY | Substantially Equivalent | |
| K901272 | ORION BLADE PLATE FOR TIBIAL OSTEOTOMY | KTT | Substantially Equivalent | |
| K901240 | ASTEL NON-METAL BACKED ACETABULAR CUP FOR CEMENTED | JDI | Substantially Equivalent | |
| K894978 | BACTERIAL FILTER | CAH | Substantially Equivalent | |
| K894906 | ANESTHESIA BREATHING BAGS SIZES 1/2, 1,2,3 LITER | BTC | Substantially Equivalent | |
| K812059 | SPHGOMOMANOMETER | DXN | Substantially Equivalent | |
| K800614 | MEDTEK #411 PORTABLE B-P INSTR. | DXN | Substantially Equivalent | |
| K800222 | MODEL 412 ELECTROFLUIDIC MANOMETER | DXW | Substantially Equivalent | |
| K781906 | BLOOD PRESSURE DEVICE, 400 SERIES | DXN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- BTCBag, Reservoir
- CAICircuit, Breathing (W Connector, Adaptor, Y Piece)
- CAHFilter, Bacterial, Breathing-Circuit
- HTYPin, Fixation, Smooth
- KWAProsthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- LWJProsthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
- DXNSystem, Measurement, Blood-Pressure, Non-Invasive
- DXWSystem, Phonocatheter, Intracavitary
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