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FDA 510(k)

FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B

K-Number: K081445 · 2008-08-11

Decision Date2008-08-11
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B 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 2008-08-11 under 510(k) number K081445. 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 FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B?

FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B is a medical device that received FDA 510(k) clearance on 2008-08-11. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K081445.

When did FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B receive FDA 510(k) clearance?

FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B received FDA 510(k) clearance on 2008-08-11, under 510(k) number K081445.

Who is the listed applicant for FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B?

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 FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B?

The FDA product code for FORA COMFORTSCAN EAR THERMOMETER, MODELS TD-1261A; TD-1261B 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 Taidoc Technology Corporation 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 121 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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