510(k) K963623

SPYROFLEX PIGMENTED WOUND DRESSING by Polymedica Industries, Inc. — Product Code MGP

K963623 is an FDA 510(k) premarket notification submitted by Polymedica Industries, Inc. for the device "SPYROFLEX PIGMENTED WOUND DRESSING". The FDA issued a decision of Substantially Equivalent on October 25, 1996. The device falls under product code MGP (Dressing, Wound And Burn, Occlusive), a Class U device. Polymedica Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1996
Date Received
September 11, 1996
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