510(k) K803118
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 22, 1980
- Date Received
- December 10, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Surgical Instrument, Disposable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type