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FDA 510(k)

BLOOD PRESSURE KIT, WELL-BE 669

K-Number: K761274 · 1977-01-05

Decision Date1977-01-05
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE KIT, WELL-BE 669 is the device name listed in this FDA 510(k) record. The listed applicant is Pearlduck, Inc.. It received FDA 510(k) clearance on 1977-01-05 under 510(k) number K761274. 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 BLOOD PRESSURE KIT, WELL-BE 669?

BLOOD PRESSURE KIT, WELL-BE 669 is a medical device that received FDA 510(k) clearance on 1977-01-05. The listed applicant is Pearlduck, Inc.. The 510(k) number is K761274.

When did BLOOD PRESSURE KIT, WELL-BE 669 receive FDA 510(k) clearance?

BLOOD PRESSURE KIT, WELL-BE 669 received FDA 510(k) clearance on 1977-01-05, under 510(k) number K761274.

Who is the listed applicant for BLOOD PRESSURE KIT, WELL-BE 669?

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

What is the FDA product code for BLOOD PRESSURE KIT, WELL-BE 669?

The FDA product code for BLOOD PRESSURE KIT, WELL-BE 669 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.

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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