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FDA 510(k)

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)

K-Number: K240077 · 2024-08-20

ApplicantCovidien
Decision Date2024-08-20
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is the device name listed in this FDA 510(k) record. The listed applicant is Covidien. It received FDA 510(k) clearance on 2024-08-20 under 510(k) number K240077. 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 Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) is a medical device that received FDA 510(k) clearance on 2024-08-20. The listed applicant is Covidien. The 510(k) number is K240077.

When did Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) receive FDA 510(k) clearance?

Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) received FDA 510(k) clearance on 2024-08-20, under 510(k) number K240077.

Who is the listed applicant for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

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

What is the FDA product code for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)?

The FDA product code for Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044) 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 Covidien 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.

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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.