ClearanceBrief
Company ยท US

Bausch & Lomb Pharmaceutical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1990. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MOECollagen Corneal Shield5
HQJImplant, Absorbable, (Scleral Buckling Methods)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 9, 1990K884962ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA
Bausch & Lomb Pharmaceutical, Inc.
MOE
Feb 13, 1989K884961ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL
Bausch & Lomb Pharmaceutical, Inc.
MOE
Feb 13, 1989K884960ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
Bausch & Lomb Pharmaceutical, Inc.
MOE
Nov 29, 1988K884364LABELING CHANGES TO BIO-COR EXT COLLANGEN CORNEAL
Bausch & Lomb Pharmaceutical, Inc.
MOE
Nov 29, 1988K884363LABELING CHANGES TO BIO-COR II COLLANGEN CORNEAL
Bausch & Lomb Pharmaceutical, Inc.
MOE
Nov 29, 1988K884362LABELING CHANGES TO FYODOROV COLLAGEN CORNEAL SHLD
Bausch & Lomb Pharmaceutical, Inc.
HQJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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