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FDA 510(k)

NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER

K-Number: K122221 · 2013-03-29

ApplicantTaidoc Technology Corporation
Decision Date2013-03-29
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2013-03-29 under 510(k) number K122221. 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 NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER?

NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER is a medical device that received FDA 510(k) clearance on 2013-03-29. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K122221.

When did NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER receive FDA 510(k) clearance?

NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER received FDA 510(k) clearance on 2013-03-29, under 510(k) number K122221.

Who is the listed applicant for NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER?

The FDA product code for NEXUS IR30 NON-CONTACT INFRARED FOREHEAD THERMOMETER is FLL.

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Related Devices (Code: FLL)

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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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