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FDA 510(k)

DIGITAL FEVER THERMOMETER MODEL MC-5

K-Number: K871888 · 1987-06-17

Decision Date1987-06-17
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL FEVER THERMOMETER MODEL MC-5 is the device name listed in this FDA 510(k) record. The listed applicant is Omron Electronics, Inc.. It received FDA 510(k) clearance on 1987-06-17 under 510(k) number K871888. 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 DIGITAL FEVER THERMOMETER MODEL MC-5?

DIGITAL FEVER THERMOMETER MODEL MC-5 is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is Omron Electronics, Inc.. The 510(k) number is K871888.

When did DIGITAL FEVER THERMOMETER MODEL MC-5 receive FDA 510(k) clearance?

DIGITAL FEVER THERMOMETER MODEL MC-5 received FDA 510(k) clearance on 1987-06-17, under 510(k) number K871888.

Who is the listed applicant for DIGITAL FEVER THERMOMETER MODEL MC-5?

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

What is the FDA product code for DIGITAL FEVER THERMOMETER MODEL MC-5?

The FDA product code for DIGITAL FEVER THERMOMETER MODEL MC-5 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 Omron Electronics, 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.

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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.

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