meddevicedb.com FDA Device Reference

SPAC TM T3 UPTAKE KIT

K770033 Class II Traditional
Decision Date
1977-02-07
Sponsor / Applicant
Mallinckrodt Critical Care

Technical Specification

510(k) Submission ID K770033
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1977-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPAC TM T3 UPTAKE KIT received FDA 510(k) clearance under submission number K770033, sponsored by Mallinckrodt Critical Care. 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 1977-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.