510(k) K933308
K933308 is an FDA 510(k) premarket notification submitted by Dynarex Corp. for the device "DYNAREX GAUZE SPONGE OR PADS". The FDA issued a decision of Substantially Equivalent on December 22, 1993. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Dynarex Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1993
- Date Received
- July 7, 1993
- 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