510(k) K901990

VINYL SILICONE ELASTOMER MATERIAL by Crown Delta Corp. — Product Code MDA

K901990 is an FDA 510(k) premarket notification submitted by Crown Delta Corp. for the device "VINYL SILICONE ELASTOMER MATERIAL". The FDA issued a decision of Substantially Equivalent on September 14, 1990. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Crown Delta Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 14, 1990
Date Received
May 2, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Elastomer, Silicone, For Scar Management
Device Class
Class I
Regulation Number
878.4025
Review Panel
SU
Submission Type