510(k) K946326
K946326 is an FDA 510(k) premarket notification submitted by Dumex Medical Surgical Products, Ltd. for the device "DUTEX GAUZE BANDAGE". The FDA issued a decision of Substantially Equivalent on January 24, 1995. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Dumex Medical Surgical Products, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 24, 1995
- Date Received
- December 22, 1994
- 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