meddevicedb.com FDA Device Reference

BLOOD GAS CONTROL PROD. NO. BG-1, BG-2

K801449 Class I Traditional
Decision Date
1980-07-21
Sponsor / Applicant
Health Diagnostics Corp.

Technical Specification

510(k) Submission ID K801449
Product Code JJS
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1660
Decision Date 1980-07-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BLOOD GAS CONTROL PROD. NO. BG-1, BG-2 received FDA 510(k) clearance under submission number K801449, sponsored by Health Diagnostics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1980-07-21.

Classification & Regulation

This clearance is catalogued under FDA product code JJS and 21 CFR 862.1660, within the Clinical Chemistry review panel as a Class I device.