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FDA 510(k)

NORELCO DIGITAL BLOOD PRESSURE METER HC3001

K-Number: K855048 · 1986-11-17

ApplicantPhilips Park
Decision Date1986-11-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NORELCO DIGITAL BLOOD PRESSURE METER HC3001 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Park. It received FDA 510(k) clearance on 1986-11-17 under 510(k) number K855048. 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 DIGITAL BLOOD PRESSURE METER HC3001?

NORELCO DIGITAL BLOOD PRESSURE METER HC3001 is a medical device that received FDA 510(k) clearance on 1986-11-17. The listed applicant is Philips Park. The 510(k) number is K855048.

When did NORELCO DIGITAL BLOOD PRESSURE METER HC3001 receive FDA 510(k) clearance?

NORELCO DIGITAL BLOOD PRESSURE METER HC3001 received FDA 510(k) clearance on 1986-11-17, under 510(k) number K855048.

Who is the listed applicant for NORELCO DIGITAL BLOOD PRESSURE METER HC3001?

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

What is the FDA product code for NORELCO DIGITAL BLOOD PRESSURE METER HC3001?

The FDA product code for NORELCO DIGITAL BLOOD PRESSURE METER HC3001 is DXN.

Related Clinical Trials

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.

Other records listing Philips Park 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.

View all 11 devices →

Related Devices (Code: DXN)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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