510(k) K953885

SPYROFLEX SKIN PROTECTOR by Polymedica Industries, Inc. — Product Code MGP

K953885 is an FDA 510(k) premarket notification submitted by Polymedica Industries, Inc. for the device "SPYROFLEX SKIN PROTECTOR". The FDA issued a decision of Substantially Equivalent on November 29, 1995. 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
November 29, 1995
Date Received
August 17, 1995
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