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PHYSICIAN BARRIER GLOVE, SURGICAL

K901221 Class I Traditional
Decision Date
1990-07-10
Sponsor / Applicant
Dynamic Marketing Ent.

Technical Specification

510(k) Submission ID K901221
Product Code LYU
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1990-07-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHYSICIAN BARRIER GLOVE, SURGICAL received FDA 510(k) clearance under submission number K901221, sponsored by Dynamic Marketing Ent.. 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 1990-07-10.

Classification & Regulation

This clearance is catalogued under FDA product code LYU and 21 CFR 878.4040, within the General, Plastic Surgery review panel as a Class I device.