Bausch & Lomb Pharmaceutical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bausch & Lomb Pharmaceutical, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Bausch & Lomb Pharmaceutical, Inc. has 6 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Historical record: 6 cleared submissions from 1988 to 1990. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bausch & Lomb Pharmaceutical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bausch & Lomb Pharmaceutical, Inc.
6 devices
Cleared
Feb 09, 1990
ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA
Ophthalmic
448d
Cleared
Feb 13, 1989
ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
Ophthalmic
87d
Cleared
Feb 13, 1989
ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL
Ophthalmic
87d
Cleared
Nov 29, 1988
LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD
Ophthalmic
40d
Cleared
Nov 29, 1988
LABELING CHANGES TO BIO-COR II COLLANGEN CORNEAL
Ophthalmic
40d
Cleared
Nov 29, 1988
LABELING CHANGES TO BIO-COR EXT COLLANGEN CORNEAL
Ophthalmic
40d