Med-West, Inc.
Mchenry, IL, US
Med-West, Inc. appears in FDA device records in Mchenry, IL. FDA records list 11 510(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
- 11
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 11 510(k) clearances for Med-West, Inc. between 1983 and 1988. The busiest year on record is 1983, with 4. The most recent is 1988, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1983 | 4 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 1 |
| 1987 | 2 |
| 1988 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K880877 | CONTRAST INJECTION DEVICE | DXT | Substantially Equivalent | |
| K880398 | POWER TOILET ELEVATOR | INO | Substantially Equivalent | |
| K874470 | MWI 400 WOUND DRESSING | NAD | Substantially Equivalent for Some Indications | |
| K872724 | SHEATH/DILATORS | DRE | Substantially Equivalent | |
| K854612 | ACUTE HEMODIALYSIS TRAY, CAT.#09-9540-7 | LFK | Unknown | |
| K852162 | MNI 400 INJECTION CAPS | LFJ | Substantially Equivalent | |
| K842342 | MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN | Unknown | ||
| K832124 | CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI | DWF | Substantially Equivalent | |
| K831828 | TEFLON FEMORAL CATHETER MWI 100,10 & | LFK | Substantially Equivalent | |
| K831440 | SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 | FIQ | Substantially Equivalent | |
| K831401 | SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS | FIQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
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