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FDA 510(k)

ANEROID BLOOD PRESSURE CUFF #HC1400

K-Number: K830686 · 1983-05-18

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

Device Summary

ANEROID BLOOD PRESSURE CUFF #HC1400 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 K830686. 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 ANEROID BLOOD PRESSURE CUFF #HC1400?

ANEROID BLOOD PRESSURE CUFF #HC1400 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 K830686.

When did ANEROID BLOOD PRESSURE CUFF #HC1400 receive FDA 510(k) clearance?

ANEROID BLOOD PRESSURE CUFF #HC1400 received FDA 510(k) clearance on 1983-05-18, under 510(k) number K830686.

Who is the listed applicant for ANEROID BLOOD PRESSURE CUFF #HC1400?

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 ANEROID BLOOD PRESSURE CUFF #HC1400?

The FDA product code for ANEROID BLOOD PRESSURE CUFF #HC1400 is DXN.

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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.

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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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