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FDA 510(k)

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES

K-Number: K062016 · 2006-10-27

ApplicantChoice Smart Health Care Co. , Ltd.
Decision Date2006-10-27
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Choice Smart Health Care Co. , Ltd.. It received FDA 510(k) clearance on 2006-10-27 under 510(k) number K062016. 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 RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES?

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES is a medical device that received FDA 510(k) clearance on 2006-10-27. The listed applicant is Choice Smart Health Care Co. , Ltd.. The 510(k) number is K062016.

When did RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES receive FDA 510(k) clearance?

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES received FDA 510(k) clearance on 2006-10-27, under 510(k) number K062016.

Who is the listed applicant for RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES?

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

What is the FDA product code for RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES?

The FDA product code for RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES is FLL.

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Other records listing Choice Smart Health Care Co. , Ltd. as applicant

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Related Devices (Code: FLL)

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Official Source

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