meddevicedb.com FDA Device Reference

WESTMED CONDESATE COLLECTION TRAP

K954271 Class II Traditional
Decision Date
1995-12-28
Sponsor / Applicant
Westmed Intl.

Technical Specification

510(k) Submission ID K954271
Product Code CAW
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5440
Decision Date 1995-12-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WESTMED CONDESATE COLLECTION TRAP received FDA 510(k) clearance under submission number K954271, sponsored by Westmed Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1995-12-28.

Classification & Regulation

This clearance is catalogued under FDA product code CAW and 21 CFR 868.5440, within the Anesthesiology review panel as a Class II device.