meddevicedb.com FDA Device Reference

ATRAUMAX(TM) SURGICAL CLAMPS

K891296 Class II Traditional
Decision Date
1989-06-07
Sponsor / Applicant
Applied Vascular Devices, Inc.

Technical Specification

510(k) Submission ID K891296
Product Code DXC
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4450
Decision Date 1989-06-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ATRAUMAX(TM) SURGICAL CLAMPS received FDA 510(k) clearance under submission number K891296, sponsored by Applied Vascular Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-06-07.

Classification & Regulation

This clearance is catalogued under FDA product code DXC and 21 CFR 870.4450, within the Cardiovascular review panel as a Class II device.