NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER
K-Number: K855177 · 1986-11-07
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Device Summary
Frequently Asked Questions
What is the NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER?
NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER is a medical device that received FDA 510(k) clearance on 1986-11-07. The listed applicant is Philips Park. The 510(k) number is K855177.
When did NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER receive FDA 510(k) clearance?
NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER received FDA 510(k) clearance on 1986-11-07, under 510(k) number K855177.
Who is the listed applicant for NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER?
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 ELECTRNIC DIGITAL BLOOD PRESSURE METER?
The FDA product code for NORELCO ELECTRNIC DIGITAL BLOOD PRESSURE METER 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.
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
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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