Clearance Summary
MANUAL SURGICAL INSTRUMENTS received FDA 510(k) clearance under submission number K920263, sponsored by Phoenix Instruments Div.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1992-05-06.
- Submission: K920263
- Applicant / Sponsor: Phoenix Instruments Div.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4800
- Decision date: 1992-05-06
Classification & Regulation
This clearance is catalogued under FDA product code KDC and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.