meddevicedb.com FDA Device Reference

PINT BOTTLE WELL

K781364 Class I Traditional
Decision Date
1978-10-17
Sponsor / Applicant
Baxa Corp., Sub. of Cook Group, Inc.

Technical Specification

510(k) Submission ID K781364
Product Code KYX
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6430
Decision Date 1978-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PINT BOTTLE WELL received FDA 510(k) clearance under submission number K781364, sponsored by Baxa Corp., Sub. of Cook Group, Inc.. 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 1978-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code KYX and 21 CFR 880.6430, within the General Hospital review panel as a Class I device.