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FDA 510(k)

NORELCO ELECTRONIC DIGITAL BP METER

K-Number: K841489 · 1984-04-10

ApplicantNorth American Philips Corp.
Decision Date1984-04-10
Product Code
DecisionUnknown

Device Summary

NORELCO ELECTRONIC DIGITAL BP 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 1984-04-10 under 510(k) number K841489. FDA Decision: Unknown.

Frequently Asked Questions

What is the NORELCO ELECTRONIC DIGITAL BP METER?

NORELCO ELECTRONIC DIGITAL BP METER is a medical device that received FDA 510(k) clearance on 1984-04-10. The listed applicant is North American Philips Corp.. The 510(k) number is K841489.

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

NORELCO ELECTRONIC DIGITAL BP METER received FDA 510(k) clearance on 1984-04-10, under 510(k) number K841489.

Who is the listed applicant for NORELCO ELECTRONIC DIGITAL BP METER?

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

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Other records listing North American Philips Corp. as applicant

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.

K842486ELECTRONIC DIGITAL BP METER HC 3001K833755ELECTRONIC DIGITAL FEVER THERMOMETERK830715NORELCO VIBRATING BOARD V900K830684NORELCO ELECTRONIC DIGITAL BLOOD PRESSK830686ANEROID BLOOD PRESSURE CUFF #HC1400K830687NORELCO ELECTRONIC ANALOG BLOOD PRESS

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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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