510(k) K953618
K953618 is an FDA 510(k) premarket notification submitted by Polymedica Industries, Inc. for the device "SPYROFLEX WOUND DRESSING". The FDA issued a decision of SN on August 21, 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
- SN ()
- Decision Date
- August 21, 1995
- Date Received
- August 3, 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