Clearance Summary
POWDER-FREE DURAPRENE STERILE SYNTHETIC SURGICAL GLOVES received FDA 510(k) clearance under submission number K971381, sponsored by Allegiance Healthcare Corp.. 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 1997-07-09.
- Submission: K971381
- Applicant / Sponsor: Allegiance Healthcare Corp.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class I
- Regulation citation: 21 CFR 878.4460
- Decision date: 1997-07-09
Classification & Regulation
This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.