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FDA 510(k)

ELECTRONIC DIGITAL FEVER THERMOMETER

K-Number: K833755 · 1984-01-30

ApplicantNorth American Philips Corp.
Decision Date1984-01-30
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ELECTRONIC DIGITAL FEVER THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is North American Philips Corp.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K833755. 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 ELECTRONIC DIGITAL FEVER THERMOMETER?

ELECTRONIC DIGITAL FEVER THERMOMETER is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is North American Philips Corp.. The 510(k) number is K833755.

When did ELECTRONIC DIGITAL FEVER THERMOMETER receive FDA 510(k) clearance?

ELECTRONIC DIGITAL FEVER THERMOMETER received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833755.

Who is the listed applicant for ELECTRONIC DIGITAL FEVER THERMOMETER?

The FDA 510(k) record lists North American Philips Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTRONIC DIGITAL FEVER THERMOMETER?

The FDA product code for ELECTRONIC DIGITAL FEVER THERMOMETER is FLL.

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Related Devices (Code: 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.

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