510(k) K902010

VISI - STICK OPHTHALMIC SUTURE RETAINER TAPE by Visitec Co. — Product Code KGX

K902010 is an FDA 510(k) premarket notification submitted by Visitec Co. for the device "VISI - STICK OPHTHALMIC SUTURE RETAINER TAPE". The FDA issued a decision of Substantially Equivalent on June 20, 1990. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Visitec Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1990
Date Received
May 3, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tape And Bandage, Adhesive
Device Class
Class I
Regulation Number
880.5240
Review Panel
SU
Submission Type