Atlas FDA

ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL

FDA 510(k) clearance K884960 · decided 1989-02-13

Clearance details

K-number
K884960
Device name
ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL
Applicant
Bausch & Lomb Pharmaceutical, Inc.
Decision
Substantially Equivalent
Date received
1988-11-18
Decision date
1989-02-13
Days to decision
87 days
Clearance type
Traditional
Product code
MOE
Device class
1
Regulation number
886.4750
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Clearwater, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
BIO-COR COLLAGEN CORNEAL SHIELD (K944872)Bausch & Lomb Healthcare and Optics Worldwide1995-07-26
MEDILENS-CS CORNEAL SHIELD (K915861)Chiron Ophthalmics1992-03-06
SOFTSHIELD(TM) 12, 24, 72 COLLAGEN CORNEAL SHIELDS (K914529)Oasis Medical, Inc.1991-11-13
COLLAGEN SHIELD FOR ACUTE CARE (K913148)Vitaphore Corp.1991-10-15
COLLAGEN SHIELD, VARIOUS MODELS (K905825)Chiron Ophthalmics1991-06-10
COLLAGEN SHIELD FOR ACUTE CARE (K902558)Vitaphore Corp.1990-08-17
MEDILENS(TM) CORNEAL SHIELD (K901880)Chiron Ophthalmics1990-07-02
IM COLLAGEN SHIELD (K896449)Intermedical, Inc.1990-05-24
ADDIT. INDICATIONS FOR BIO-COR EXT COLLAGEN CORNEA (K884962)Bausch & Lomb Pharmaceutical, Inc.1990-02-09
COI 72 HR COLLAGEN SHIELD (K885015)Chiron Ophthalmics1989-06-23
ADDIT. INDICATIONS FOR BIO-COR II COLLAGEN CORNEAL (K884961)Bausch & Lomb Pharmaceutical, Inc.1989-02-13
COI 24 HR COLLAGEN SHIELD (K885016)Chiron Ophthalmics1989-02-01

Recalls involving this device

No recalls on record reference this clearance.