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FDA 510(k)

NORELCO DELUXE DIGITAL BLOOD PRESSURE

K-Number: K830685 · 1983-05-18

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

Device Summary

NORELCO DELUXE DIGITAL BLOOD PRESSURE 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 K830685. 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 DELUXE DIGITAL BLOOD PRESSURE?

NORELCO DELUXE DIGITAL BLOOD PRESSURE 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 K830685.

When did NORELCO DELUXE DIGITAL BLOOD PRESSURE receive FDA 510(k) clearance?

NORELCO DELUXE DIGITAL BLOOD PRESSURE received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830685.

Who is the listed applicant for NORELCO DELUXE DIGITAL BLOOD PRESSURE?

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 DELUXE DIGITAL BLOOD PRESSURE?

The FDA product code for NORELCO DELUXE DIGITAL BLOOD PRESSURE is DXN.

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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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