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FDA 510(k)

DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4.

K-Number: K072641 · 2007-11-01

ApplicantFamidoc Technology Co., Ltd.
Decision Date2007-11-01
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4. is the device name listed in this FDA 510(k) record. The listed applicant is Famidoc Technology Co., Ltd.. It received FDA 510(k) clearance on 2007-11-01 under 510(k) number K072641. 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 ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4.?

DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4. is a medical device that received FDA 510(k) clearance on 2007-11-01. The listed applicant is Famidoc Technology Co., Ltd.. The 510(k) number is K072641.

When did DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4. receive FDA 510(k) clearance?

DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4. received FDA 510(k) clearance on 2007-11-01, under 510(k) number K072641.

Who is the listed applicant for DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4.?

The FDA 510(k) record lists Famidoc Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4.?

The FDA product code for DIGITAL ELECTRONIC THERMOMETER, MODEL: FDTH-V0-1 THRU 4. is FLL.

Related Clinical Trials

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Other records listing Famidoc Technology 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.

K212918Heat StimPlusK113010FDES100(TENS AND EMS STIMULATOR, FDES102(ED402) TENS STIMULATORK113761INFRARED THERMOMETERK052849INFRARED THERMOMETER, FDIR-V1

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

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