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FDA 510(k)

HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF

K-Number: K032821 · 2003-12-05

Decision Date2003-12-05
Product CodeNPP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF is the device name listed in this FDA 510(k) record. The listed applicant is Hygia Health Services, Inc.. It received FDA 510(k) clearance on 2003-12-05 under 510(k) number K032821. The device is classified under product code NPP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF?

HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2003-12-05. The listed applicant is Hygia Health Services, Inc.. The 510(k) number is K032821.

When did HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF receive FDA 510(k) clearance?

HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2003-12-05, under 510(k) number K032821.

Who is the listed applicant for HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF?

The FDA 510(k) record lists Hygia Health Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF?

The FDA product code for HYGIA HEALTH SERVICES REPROCESSED BLOOD PRESSURE CUFF is NPP.

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 Hygia Health Services, Inc. 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.

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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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