FDA 510(k)

CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413

K-Number: K070342 · 2007-03-19

Decision Date2007-03-19

Product CodeFLL

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413 is the device name listed in this FDA 510(k) record. The listed applicant is American I.V. Products, Inc.. It received FDA 510(k) clearance on 2007-03-19 under 510(k) number K070342. 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 CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413?

CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413 is a medical device that received FDA 510(k) clearance on 2007-03-19. The listed applicant is American I.V. Products, Inc.. The 510(k) number is K070342.

When did CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413 receive FDA 510(k) clearance?

CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413 received FDA 510(k) clearance on 2007-03-19, under 510(k) number K070342.

Who is the listed applicant for CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413?

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

What is the FDA product code for CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413?

The FDA product code for CLINICAL ELECTRONIC THERMOMETER, MODELS TP11403 THROUGH TP11413 is FLL.

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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.