510(k) K990875
K990875 is an FDA 510(k) premarket notification submitted by Dermaphylyx, Inc. for the device "DERMAPHYLYX FILM WOUND DRESSING AND HEALIAN FILM WOUND DRESSING". The FDA issued a decision of SN on May 27, 1999. The device falls under product code MGP (Dressing, Wound And Burn, Occlusive), a Class U device. Dermaphylyx, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- May 27, 1999
- Date Received
- March 16, 1999
- 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