FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING)

K Number: K901879 · Decision Jun 22, 1990
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
34
Review Days
57

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Basic Information

Device Name
INTRASITE HYDROCOLLOID DRESSING (REVISED LABELING)
K Number
K901879
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Smith & Nephew United, Inc.
Date Received
April 26, 1990
Decision Date
June 22, 1990
Product Code
KGX
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KGX Tape And Bandage, Adhesive

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KGX), ordered by most recent decision date.

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Other Clearances by Smith & Nephew United, Inc.

K Number Device Name
K963096 ALLEVYN HYDRO POLY DRESSING ND ALL TRAC DRESSING
K961775 PROFORE FOUR-LAYER BANDAGE SYSTEM KIT
K945330 ALLEVYN ADHESIVE
K943619 CAVI-CARE CONFORMING FOAM DRESSING
K942748 INTRASITE
K935705 ALLEVYN ISLAND WOUND DRESSING
K935803 CICA-CARE SILICONE GEL SHEET
K932263 SOLOSITE DERMAL WOUND GEL
K926508 INTRASITE GEL
K922897 STRAPPAL
Search all 34 clearances from Smith & Nephew United, Inc. →