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GLOVES, VINYL EXAMINATION

K781820 Class I Traditional
Decision Date
1978-12-07
Sponsor / Applicant
Phoenix Glove Co.

Technical Specification

510(k) Submission ID K781820
Product Code FMC
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1978-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GLOVES, VINYL EXAMINATION received FDA 510(k) clearance under submission number K781820, sponsored by Phoenix Glove Co.. 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 1978-12-07.

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.