Promedica Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K913101PETERS CARDIOFLON(TM) SUTUREAugust 12, 1992
K913102PETERS CARDIONYL(TM) SUTUREAugust 3, 1992
K892768PATIENT EXAMINATION GLOVES (POLY)June 14, 1989
K883412THE CARPENTIER TRANS-MITRAL VENTRICULAR VENT(TM)February 8, 1989
K882882C-MASKAugust 10, 1988
K882883C-MASK(FLAT)August 10, 1988