Bausch & Lomb Pharmaceutical, Inc.
Bausch & Lomb Pharmaceutical, Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 1990.
Top product codes for Bausch & Lomb Pharmaceutical, Inc.
Recent clearances by Bausch & Lomb Pharmaceutical, Inc.
- K884962 — ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA
- K884960 — ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
- K884961 — ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL
- K884362 — LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD
- K884363 — LABELING CHANGES TO BIO-COR II COLLANGEN CORNEAL
- K884364 — LABELING CHANGES TO BIO-COR EXT COLLANGEN CORNEAL
Data sourced from openFDA. This site is unofficial and independent of the FDA.