Sterling Drug, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K901369GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE IIJune 5, 1990
K896110BIOBRANE(R) IINovember 28, 1989
K875275WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMERJanuary 27, 1988
K840260PERIOGRAF DURAPATITE 40-60 MESHApril 5, 1984
K820164EMPTY STERILE CARPUJECTFebruary 24, 1982
K820023CONAGRAF TM DURAPATITE CONESFebruary 24, 1982
K813257ALVEOGRAF DURAPATITE(18-40 MESH)January 5, 1982
K813070PERIOGRAFNovember 20, 1981
K780209DILUTION SPIKEApril 10, 1978