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MEDSPEC PACKING GAUZE

K800281 Class I Traditional
Decision Date
1980-03-12
Sponsor / Applicant
Medspec Corp.

Technical Specification

510(k) Submission ID K800281
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1980-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDSPEC PACKING GAUZE received FDA 510(k) clearance under submission number K800281, sponsored by Medspec Corp.. 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 1980-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code GDY and 21 CFR 878.4450, within the General, Plastic Surgery review panel as a Class I device.