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FDA 510(k)

TERUMO DIGITAL CLINICAL THERMOMETER

K-Number: K841740 · 1984-07-18

Decision Date1984-07-18
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TERUMO DIGITAL CLINICAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1984-07-18 under 510(k) number K841740. 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 TERUMO DIGITAL CLINICAL THERMOMETER?

TERUMO DIGITAL CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1984-07-18. The listed applicant is Terumo Medical Corp.. The 510(k) number is K841740.

When did TERUMO DIGITAL CLINICAL THERMOMETER receive FDA 510(k) clearance?

TERUMO DIGITAL CLINICAL THERMOMETER received FDA 510(k) clearance on 1984-07-18, under 510(k) number K841740.

Who is the listed applicant for TERUMO DIGITAL CLINICAL THERMOMETER?

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

What is the FDA product code for TERUMO DIGITAL CLINICAL THERMOMETER?

The FDA product code for TERUMO DIGITAL CLINICAL 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 Terumo Medical 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.

View all 143 devices →

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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