510(k) K942339

SKIN NEUVEAU SCAR TREATMENT by Puritas Health Care, Inc. — Product Code MDA

K942339 is an FDA 510(k) premarket notification submitted by Puritas Health Care, Inc. for the device "SKIN NEUVEAU SCAR TREATMENT". The FDA issued a decision of Substantially Equivalent on November 28, 1994. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Puritas Health Care, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 28, 1994
Date Received
May 16, 1994
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