Sterling Drug, Inc.
Sterling Drug, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1990.
Top product codes for Sterling Drug, Inc.
Recent clearances by Sterling Drug, Inc.
- K901369 — GREEN LABEL BIOBRANE II AND RED LABEL BIOBRANE II
- K896110 — BIOBRANE(R) II
- K875275 — WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMER
- K840260 — PERIOGRAF DURAPATITE 40-60 MESH
- K820023 — CONAGRAF TM DURAPATITE CONES
- K820164 — EMPTY STERILE CARPUJECT
- K813257 — ALVEOGRAF DURAPATITE(18-40 MESH)
- K813070 — PERIOGRAF
- K780209 — DILUTION SPIKE
Data sourced from openFDA. This site is unofficial and independent of the FDA.