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MEDLINE PROHIBIT SERIES SURGICAL MASK WITH FLUID SHIELD

K991559 Class II Traditional
Decision Date
1999-08-23
Sponsor / Applicant
Medline Industries, Inc.

Technical Specification

510(k) Submission ID K991559
Product Code FXX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4040
Decision Date 1999-08-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDLINE PROHIBIT SERIES SURGICAL MASK WITH FLUID SHIELD received FDA 510(k) clearance under submission number K991559, sponsored by Medline Industries, 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 1999-08-23.

Classification & Regulation

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