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FDA 510(k)

NORELCO ELECTRONIC DIGITAL THERMOMETER

K-Number: K811672 · 1981-06-26

ApplicantNorth American Philips Corp.
Decision Date1981-06-26
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NORELCO ELECTRONIC DIGITAL 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 1981-06-26 under 510(k) number K811672. 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 NORELCO ELECTRONIC DIGITAL THERMOMETER?

NORELCO ELECTRONIC DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1981-06-26. The listed applicant is North American Philips Corp.. The 510(k) number is K811672.

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

NORELCO ELECTRONIC DIGITAL THERMOMETER received FDA 510(k) clearance on 1981-06-26, under 510(k) number K811672.

Who is the listed applicant for NORELCO ELECTRONIC DIGITAL 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 NORELCO ELECTRONIC DIGITAL THERMOMETER?

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

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Other records listing North American Philips Corp. as applicant

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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

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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