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FDA 510(k)

TEMPERATURE MONITOR (W/PROBE)

K-Number: K792257 · 1979-12-04

Decision Date1979-12-04
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPERATURE MONITOR (W/PROBE) is the device name listed in this FDA 510(k) record. The listed applicant is Biotronex Laboratory, Inc.. It received FDA 510(k) clearance on 1979-12-04 under 510(k) number K792257. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPERATURE MONITOR (W/PROBE)?

TEMPERATURE MONITOR (W/PROBE) is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Biotronex Laboratory, Inc.. The 510(k) number is K792257.

When did TEMPERATURE MONITOR (W/PROBE) receive FDA 510(k) clearance?

TEMPERATURE MONITOR (W/PROBE) received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792257.

Who is the listed applicant for TEMPERATURE MONITOR (W/PROBE)?

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

What is the FDA product code for TEMPERATURE MONITOR (W/PROBE)?

The FDA product code for TEMPERATURE MONITOR (W/PROBE) is FLL.

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.

Related Devices (Code: FLL)

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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