510(k) K884960

ADDIT. INDICATION FOR FYODOROV COLLAGEN CORNEAL by Bausch & Lomb Pharmaceutical, Inc. — Product Code MOE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 13, 1989
Date Received
November 18, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Collagen Corneal Shield
Device Class
Class I
Regulation Number
886.4750
Review Panel
OP
Submission Type