SHIELD DISPOSABLE BLOOD PRESSURE CUFF
K-Number: K801568 · 1980-07-28
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Device Summary
Frequently Asked Questions
What is the SHIELD DISPOSABLE BLOOD PRESSURE CUFF?
SHIELD DISPOSABLE BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is American Convertors Div., American Pharmaseal. The 510(k) number is K801568.
When did SHIELD DISPOSABLE BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
SHIELD DISPOSABLE BLOOD PRESSURE CUFF received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801568.
Who is the listed applicant for SHIELD DISPOSABLE BLOOD PRESSURE CUFF?
The FDA 510(k) record lists American Convertors Div., American Pharmaseal as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SHIELD DISPOSABLE BLOOD PRESSURE CUFF?
The FDA product code for SHIELD DISPOSABLE BLOOD PRESSURE CUFF is DXQ.
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 American Convertors Div., American Pharmaseal 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: DXQ)
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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