510(k) K960615
K960615 is an FDA 510(k) premarket notification submitted by Certified Safety Mfg., Inc. for the device "GAUZE COMPRESS". The FDA issued a decision of SN on November 25, 1996. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Certified Safety Mfg., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- November 25, 1996
- Date Received
- February 13, 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