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LAPAROTOMY SPONGES

K905135 Class I Traditional
Decision Date
1991-03-06
Sponsor / Applicant
American Healthcare Corp.

Technical Specification

510(k) Submission ID K905135
Product Code GDY
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4450
Decision Date 1991-03-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LAPAROTOMY SPONGES received FDA 510(k) clearance under submission number K905135, sponsored by American Healthcare 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 1991-03-06.

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.