Company ยท US
Promedica Products, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1992. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 12, 1992 | K913101 | PETERS CARDIOFLON(TM) SUTURE Promedica Products, Inc. | GAS |
| Aug 3, 1992 | K913102 | PETERS CARDIONYL(TM) SUTURE Promedica Products, Inc. | GAR |
| Jun 14, 1989 | K892768 | PATIENT EXAMINATION GLOVES (POLY) Promedica Products, Inc. | LZA |
| Feb 8, 1989 | K883412 | THE CARPENTIER TRANS-MITRAL VENTRICULAR VENT(TM) Promedica Products, Inc. | DWF |
| Aug 10, 1988 | K882883 | C-MASK(FLAT) Promedica Products, Inc. | FXX |
| Aug 10, 1988 | K882882 | C-MASK Promedica Products, Inc. | FXX |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||