FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

SOLOSITE DERMAL WOUND GEL

K Number: K932263 · Decision Oct 1, 1993
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
144
Applicant Total
34
Review Days
164

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Basic Information

Device Name
SOLOSITE DERMAL WOUND GEL
K Number
K932263
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Smith & Nephew United, Inc.
Date Received
April 20, 1993
Decision Date
October 1, 1993
Product Code
MGQ
Advisory Committee
Unknown
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
MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

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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
K926508 INTRASITE GEL
K922897 STRAPPAL
K914147 ALLEVLYN WOUND DRESSING, MODIFICATION
Search all 34 clearances from Smith & Nephew United, Inc. →