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

SILICONE ELASTOMER PUTTY

K Number: K901991 · Decision Sep 14, 1990
Classifications
1
FEI Numbers
190
Registration Numbers
190
Same Product Code
80
Applicant Total
18
Review Days
135

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Basic Information

Device Name
SILICONE ELASTOMER PUTTY
K Number
K901991
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4025
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Crown Delta Corp.
Date Received
May 2, 1990
Decision Date
September 14, 1990
Product Code
MDA
Advisory Committee
General, Plastic Surgery
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
MDA Elastomer, Silicone, For Scar Management

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Other Clearances by Crown Delta Corp.

K Number Device Name
K122974 TRYOUT-VPS HOLDING PASTE
K041028 CROWN DELTA HYDROPHILIC IMPRESSION MATERIAL
K955288 HEARING AID IMPRESSION MATERIAL
K940132 PODIATRIC MATERIAL
K930248 VINYL POLYSILOXANE 2 COMPONENT VULCANIZING SYSTEM
K926150 VINYL ADDITION SILICONE SYSTEM
K901990 VINYL SILICONE ELASTOMER MATERIAL
K872745 VINYL POLYSILOXANE IMPRESSION SYSTEM
K871409 VINYL POLYSILOXANE IMPRESSION SYSTEM
K843145 TWO COMPONENT RTV VINYL SILICONE MATER
Search all 18 clearances from Crown Delta Corp. →