meddevicedb.com FDA Device Reference

SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES

K023236 Class I Traditional
Decision Date
2002-11-12
Sponsor / Applicant
Maxxim Medical

Technical Specification

510(k) Submission ID K023236
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2002-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SENSICARE -C SYNTHETIC POLYISOPRENE POWDER-FREE SURGICAL GLOVES received FDA 510(k) clearance under submission number K023236, sponsored by Maxxim Medical. 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 2002-11-12.

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.