510(k) K901880

MEDILENS(TM) CORNEAL SHIELD by Chiron Ophthalmics — Product Code MOE

K901880 is an FDA 510(k) premarket notification submitted by Chiron Ophthalmics for the device "MEDILENS(TM) CORNEAL SHIELD". The FDA issued a decision of Substantially Equivalent on July 2, 1990. The device falls under product code MOE (Collagen Corneal Shield), a Class I device regulated under 21 CFR 886.4750. Chiron Ophthalmics has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 2, 1990
Date Received
April 26, 1990
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