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FDA 510(k)

FLEXIBLE TIP DIGITAL THERMOMETER

K-Number: K974195 · 1998-02-04

ApplicantK-Jump Health Co., Ltd.
Decision Date1998-02-04
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE TIP DIGITAL 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 1998-02-04 under 510(k) number K974195. 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 FLEXIBLE TIP DIGITAL THERMOMETER?

FLEXIBLE TIP DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1998-02-04. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K974195.

When did FLEXIBLE TIP DIGITAL THERMOMETER receive FDA 510(k) clearance?

FLEXIBLE TIP DIGITAL THERMOMETER received FDA 510(k) clearance on 1998-02-04, under 510(k) number K974195.

Who is the listed applicant for FLEXIBLE TIP DIGITAL 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 FLEXIBLE TIP DIGITAL THERMOMETER?

The FDA product code for FLEXIBLE TIP DIGITAL THERMOMETER is FLL.

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Other records listing K-Jump Health Co., Ltd. as applicant

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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.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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