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CONPHAR EXAM. GLOVES, POLYETHYLENE

K791805 Class I Traditional
Decision Date
1979-10-01
Sponsor / Applicant
Conphar, Inc.

Technical Specification

510(k) Submission ID K791805
Product Code FMC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1979-10-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONPHAR EXAM. GLOVES, POLYETHYLENE received FDA 510(k) clearance under submission number K791805, sponsored by Conphar, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code FMC and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.