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FDA 510(k)

CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES

K-Number: K131771 · 2013-10-07

ApplicantThermomedics, Inc.
Decision Date2013-10-07
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Thermomedics, Inc.. It received FDA 510(k) clearance on 2013-10-07 under 510(k) number K131771. 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 CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES?

CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES is a medical device that received FDA 510(k) clearance on 2013-10-07. The listed applicant is Thermomedics, Inc.. The 510(k) number is K131771.

When did CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES receive FDA 510(k) clearance?

CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES received FDA 510(k) clearance on 2013-10-07, under 510(k) number K131771.

Who is the listed applicant for CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES?

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

What is the FDA product code for CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES?

The FDA product code for CAREGIVER PROFESSIONAL CLINICAL THERMOMETER, PRO-TF SERIES is FLL.

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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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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