meddevicedb.com FDA Device Reference

STOPCOCKS

K760383 Class I Traditional
Decision Date
1976-11-02
Sponsor / Applicant
B. Braun Instruments

Technical Specification

510(k) Submission ID K760383
Product Code KGZ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4200
Decision Date 1976-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STOPCOCKS received FDA 510(k) clearance under submission number K760383, sponsored by B. Braun Instruments. 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 1976-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code KGZ and 21 CFR 878.4200, within the General, Plastic Surgery review panel as a Class I device.