meddevicedb.com FDA Device Reference

C.C.-PAK

K800635 Class II Traditional
Decision Date
1980-04-10
Sponsor / Applicant
Respiratory Care, Inc.

Technical Specification

510(k) Submission ID K800635
Product Code JOL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1980-04-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C.C.-PAK received FDA 510(k) clearance under submission number K800635, sponsored by Respiratory Care, 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 1980-04-10.

Classification & Regulation

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