meddevicedb.com FDA Device Reference

MERCURY/HYDRIDE SYSTEM MHS-1

K770637 Class I Traditional
Decision Date
1977-06-23
Sponsor / Applicant
The Perkin-Elmer Corp.

Technical Specification

510(k) Submission ID K770637
Product Code DOP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2860
Decision Date 1977-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MERCURY/HYDRIDE SYSTEM MHS-1 received FDA 510(k) clearance under submission number K770637, sponsored by The Perkin-Elmer 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 1977-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code DOP and 21 CFR 862.2860, within the Clinical Chemistry review panel as a Class I device.