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DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCER

K911262 Class I Traditional
Decision Date
1991-06-20
Sponsor / Applicant
ETHICON, Inc.

Technical Specification

510(k) Submission ID K911262
Product Code GEA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1991-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCER received FDA 510(k) clearance under submission number K911262, sponsored by ETHICON, 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 1991-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code GEA and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.