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THERMAJUST CIRCU-TEMP

K780543 Class I Traditional
Decision Date
1978-05-26
Sponsor / Applicant
Techhnilab Instruments, Inc.

Technical Specification

510(k) Submission ID K780543
Product Code JRQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2050
Decision Date 1978-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERMAJUST CIRCU-TEMP received FDA 510(k) clearance under submission number K780543, sponsored by Techhnilab Instruments, Inc.. 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 1978-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code JRQ and 21 CFR 862.2050, within the Clinical Chemistry review panel as a Class I device.