510(k) K901879

INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING) by Smith & Nephew United, Inc. — Product Code KGX

K901879 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING)". The FDA issued a decision of Substantially Equivalent on June 22, 1990. The device falls under product code KGX (Tape And Bandage, Adhesive), a Class I device regulated under 21 CFR 880.5240. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 1990
Date Received
April 26, 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