BLOOD PRESSURE KIT, WELL-BE 669
K-Number: K761274 · 1977-01-05
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Device Summary
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
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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