meddevicedb.com FDA Device Reference

REGENT DISPO STERILE BIOGEL STARCH FREE SURG GLOVE

K874099 Class I Traditional
Decision Date
1987-12-14
Sponsor / Applicant
Biopro, Inc.

Technical Specification

510(k) Submission ID K874099
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1987-12-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REGENT DISPO STERILE BIOGEL STARCH FREE SURG GLOVE received FDA 510(k) clearance under submission number K874099, sponsored by Biopro, Inc.. 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 1987-12-14.

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.