510(k) K961773
K961773 is an FDA 510(k) premarket notification submitted by Derivadas Degasa S.A. DE C.V. for the device "PROTEC STERILE GAUZE SPONGE". The FDA issued a decision of Substantially Equivalent on July 29, 1996. The device falls under product code EFQ (Gauze/Sponge, Internal), a Class U device. Derivadas Degasa S.A. DE C.V. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 29, 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