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FDA 510(k)

TECHNION ELECTRONIC FEVER THERMOMETER

K-Number: K791323 · 1979-09-07

Decision Date1979-09-07
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TECHNION ELECTRONIC FEVER THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Corp.. It received FDA 510(k) clearance on 1979-09-07 under 510(k) number K791323. 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 TECHNION ELECTRONIC FEVER THERMOMETER?

TECHNION ELECTRONIC FEVER THERMOMETER is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Technicon Corp.. The 510(k) number is K791323.

When did TECHNION ELECTRONIC FEVER THERMOMETER receive FDA 510(k) clearance?

TECHNION ELECTRONIC FEVER THERMOMETER received FDA 510(k) clearance on 1979-09-07, under 510(k) number K791323.

Who is the listed applicant for TECHNION ELECTRONIC FEVER THERMOMETER?

The FDA 510(k) record lists Technicon Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TECHNION ELECTRONIC FEVER THERMOMETER?

The FDA product code for TECHNION ELECTRONIC FEVER THERMOMETER 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.

Other records listing Technicon Corp. 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: 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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