meddevicedb.com FDA Device Reference

YANKAUER SUCTION TUBE-FLEXIBLE TYPE

K896557 Class II Traditional
Decision Date
1990-02-06
Sponsor / Applicant
Westmark, Sterile Packing Systems, Inc. (Sps)

Technical Specification

510(k) Submission ID K896557
Product Code GCX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1990-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YANKAUER SUCTION TUBE-FLEXIBLE TYPE received FDA 510(k) clearance under submission number K896557, sponsored by Westmark, Sterile Packing Systems, Inc. (Sps). The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code GCX and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.