510(k) K970693

ACRYDERM GEL WOUND DRESSING by Acrymed, Inc. — Product Code MGQ

K970693 is an FDA 510(k) premarket notification submitted by Acrymed, Inc. for the device "ACRYDERM GEL WOUND DRESSING". The FDA issued a decision of SN on March 21, 1997. The device falls under product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic), a Class U device. Acrymed, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
March 21, 1997
Date Received
February 25, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type