meddevicedb.com FDA Device Reference

SUCTION CONTROL VALVE (NONADJUSTABLE) CAT.RLV-2100

K861428 Class II Traditional
Decision Date
1986-06-26
Sponsor / Applicant
American Omni Medical, Inc.

Technical Specification

510(k) Submission ID K861428
Product Code DWD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4430
Decision Date 1986-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUCTION CONTROL VALVE (NONADJUSTABLE) CAT.RLV-2100 received FDA 510(k) clearance under submission number K861428, sponsored by American Omni Medical, 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 1986-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code DWD and 21 CFR 870.4430, within the Cardiovascular review panel as a Class II device.