GSIBP BLOOD PRESSURE CUFF
K-Number: K012553 · 2001-08-17
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Device Summary
Frequently Asked Questions
What is the GSIBP BLOOD PRESSURE CUFF?
GSIBP BLOOD PRESSURE CUFF is a medical device that received FDA 510(k) clearance on 2001-08-17. The listed applicant is Globalshop, Inc.. The 510(k) number is K012553.
When did GSIBP BLOOD PRESSURE CUFF receive FDA 510(k) clearance?
GSIBP BLOOD PRESSURE CUFF received FDA 510(k) clearance on 2001-08-17, under 510(k) number K012553.
Who is the listed applicant for GSIBP BLOOD PRESSURE CUFF?
The FDA 510(k) record lists Globalshop, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GSIBP BLOOD PRESSURE CUFF?
The FDA product code for GSIBP 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.
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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