510(k) K871327
K871327 is an FDA 510(k) premarket notification submitted by Bioderm, Inc. for the device "D.R.P. THREE STEP WOUND DRESSING". The FDA issued a decision of SN on November 9, 1987. The device falls under product code FRO (Dressing, Wound, Drug), a Class U device. Bioderm, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- November 9, 1987
- Date Received
- April 3, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dressing, Wound, Drug
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type