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FDA 510(k)

THERMAJUST CIRCU-TEMP

K-Number: K780543 · 1978-05-26

Decision Date1978-05-26
Product CodeJRQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THERMAJUST CIRCU-TEMP is the device name listed in this FDA 510(k) record. The listed applicant is Techhnilab Instruments, Inc.. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780543. The device is classified under product code JRQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMAJUST CIRCU-TEMP?

THERMAJUST CIRCU-TEMP is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Techhnilab Instruments, Inc.. The 510(k) number is K780543.

When did THERMAJUST CIRCU-TEMP receive FDA 510(k) clearance?

THERMAJUST CIRCU-TEMP received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780543.

Who is the listed applicant for THERMAJUST CIRCU-TEMP?

The FDA 510(k) record lists Techhnilab Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMAJUST CIRCU-TEMP?

The FDA product code for THERMAJUST CIRCU-TEMP is JRQ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Techhnilab Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: JRQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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