meddevicedb.com FDA Device Reference

BRACHIAL PLEXUS BLOCK ANESTHESIA KIT

K761162 Class II Traditional
Decision Date
1976-12-09
Sponsor / Applicant
Arrow Intl., Inc.

Technical Specification

510(k) Submission ID K761162
Product Code CAZ
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5140
Decision Date 1976-12-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BRACHIAL PLEXUS BLOCK ANESTHESIA KIT received FDA 510(k) clearance under submission number K761162, sponsored by Arrow Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1976-12-09.

Classification & Regulation

This clearance is catalogued under FDA product code CAZ and 21 CFR 868.5140, within the Anesthesiology review panel as a Class II device.