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FDA 510(k)

TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX

K-Number: K010235 · 2001-07-09

Decision Date2001-07-09
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX is the device name listed in this FDA 510(k) record. The listed applicant is Oriental System Technology, Inc.. It received FDA 510(k) clearance on 2001-07-09 under 510(k) number K010235. 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 TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX?

TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX is a medical device that received FDA 510(k) clearance on 2001-07-09. The listed applicant is Oriental System Technology, Inc.. The 510(k) number is K010235.

When did TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX receive FDA 510(k) clearance?

TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX received FDA 510(k) clearance on 2001-07-09, under 510(k) number K010235.

Who is the listed applicant for TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX?

The FDA 510(k) record lists Oriental System Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX?

The FDA product code for TEMPTELLER INFRARED EAR THERMOMETER, MODEL CT-30/ CT-30DX 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 Oriental System Technology, Inc. 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.

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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