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FDA 510(k)

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R

K-Number: K070590 · 2007-09-11

ApplicantMicrolife Intellectual Property GmbH
Decision Date2007-09-11
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R is the device name listed in this FDA 510(k) record. The listed applicant is Microlife Intellectual Property GmbH. It received FDA 510(k) clearance on 2007-09-11 under 510(k) number K070590. 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 MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R?

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R is a medical device that received FDA 510(k) clearance on 2007-09-11. The listed applicant is Microlife Intellectual Property GmbH. The 510(k) number is K070590.

When did MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R receive FDA 510(k) clearance?

MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R received FDA 510(k) clearance on 2007-09-11, under 510(k) number K070590.

Who is the listed applicant for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R?

The FDA 510(k) record lists Microlife Intellectual Property GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R?

The FDA product code for MICROLIFE INSTANT DIGITAL ELECTRONIC THERMOMETER, MODEL MT19S1R is 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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