510(k) K961775
K961775 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "PROFORE FOUR-LAYER BANDAGE SYSTEM KIT". The FDA issued a decision of Substantially Equivalent on July 16, 1996. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 16, 1996
- Date Received
- May 8, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Gauze/Sponge, Internal
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type