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FDA 510(k)

NORELCO ANEROID BLOOD PRESSURE METER

K-Number: K811634 · 1981-06-30

ApplicantNorth American Philips Corp.
Decision Date1981-06-30
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NORELCO ANEROID BLOOD PRESSURE METER 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 1981-06-30 under 510(k) number K811634. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORELCO ANEROID BLOOD PRESSURE METER?

NORELCO ANEROID BLOOD PRESSURE METER is a medical device that received FDA 510(k) clearance on 1981-06-30. The listed applicant is North American Philips Corp.. The 510(k) number is K811634.

When did NORELCO ANEROID BLOOD PRESSURE METER receive FDA 510(k) clearance?

NORELCO ANEROID BLOOD PRESSURE METER received FDA 510(k) clearance on 1981-06-30, under 510(k) number K811634.

Who is the listed applicant for NORELCO ANEROID BLOOD PRESSURE METER?

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 ANEROID BLOOD PRESSURE METER?

The FDA product code for NORELCO ANEROID BLOOD PRESSURE METER is DXQ.

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Related Devices (Code: DXQ)

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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