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FDA 510(k)

KEJUMP DIGITAL CLINICAL THERMOMETER

K-Number: K903590 · 1990-10-22

Decision Date1990-10-22
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KEJUMP DIGITAL CLINICAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is K-Jump Health Co., Ltd.. It received FDA 510(k) clearance on 1990-10-22 under 510(k) number K903590. 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 KEJUMP DIGITAL CLINICAL THERMOMETER?

KEJUMP DIGITAL CLINICAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1990-10-22. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K903590.

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

KEJUMP DIGITAL CLINICAL THERMOMETER received FDA 510(k) clearance on 1990-10-22, under 510(k) number K903590.

Who is the listed applicant for KEJUMP DIGITAL CLINICAL THERMOMETER?

The FDA 510(k) record lists K-Jump Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for KEJUMP 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 K-Jump Health Co., Ltd. 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 25 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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