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FDA 510(k)

NORELCO ELECTRONIC ANALOG BLOOD PRESS

K-Number: K830687 · 1983-05-18

ApplicantNorth American Philips Corp.
Decision Date1983-05-18
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NORELCO ELECTRONIC ANALOG BLOOD PRESS 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 1983-05-18 under 510(k) number K830687. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORELCO ELECTRONIC ANALOG BLOOD PRESS?

NORELCO ELECTRONIC ANALOG BLOOD PRESS is a medical device that received FDA 510(k) clearance on 1983-05-18. The listed applicant is North American Philips Corp.. The 510(k) number is K830687.

When did NORELCO ELECTRONIC ANALOG BLOOD PRESS receive FDA 510(k) clearance?

NORELCO ELECTRONIC ANALOG BLOOD PRESS received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830687.

Who is the listed applicant for NORELCO ELECTRONIC ANALOG BLOOD PRESS?

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 ANALOG BLOOD PRESS?

The FDA product code for NORELCO ELECTRONIC ANALOG BLOOD PRESS is DXN.

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Other records listing North American Philips Corp. as applicant

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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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