510(k) K946292

BIODERM MEDICAL COMPOSITE WOUND DRESSING by Bioderm, Inc. — Product Code MGP

K946292 is an FDA 510(k) premarket notification submitted by Bioderm, Inc. for the device "BIODERM MEDICAL COMPOSITE WOUND DRESSING". The FDA issued a decision of Substantially Equivalent on February 6, 1995. The device falls under product code MGP (Dressing, Wound And Burn, Occlusive), a Class U device. Bioderm, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 6, 1995
Date Received
December 27, 1994
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound And Burn, Occlusive
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type