510(k) K930409

PMT(R) SILICONE GEL SHEETING MODEL 3505-1 by Pmt Corp. — Product Code MDA

K930409 is an FDA 510(k) premarket notification submitted by Pmt Corp. for the device "PMT(R) SILICONE GEL SHEETING MODEL 3505-1". The FDA issued a decision of Substantially Equivalent on September 1, 1993. The device falls under product code MDA (Elastomer, Silicone, For Scar Management), a Class I device regulated under 21 CFR 878.4025. Pmt Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 1, 1993
Date Received
January 26, 1993
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