ELECTRONIC BLOOD PRESURE MONITOR
K-Number: K102988 · 2010-11-09
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Device Summary
Frequently Asked Questions
What is the ELECTRONIC BLOOD PRESURE MONITOR?
ELECTRONIC BLOOD PRESURE MONITOR is a medical device that received FDA 510(k) clearance on 2010-11-09. The listed applicant is Shenzhen Pango Electronic Co., Ltd.. The 510(k) number is K102988.
When did ELECTRONIC BLOOD PRESURE MONITOR receive FDA 510(k) clearance?
ELECTRONIC BLOOD PRESURE MONITOR received FDA 510(k) clearance on 2010-11-09, under 510(k) number K102988.
Who is the listed applicant for ELECTRONIC BLOOD PRESURE MONITOR?
The FDA 510(k) record lists Shenzhen Pango Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ELECTRONIC BLOOD PRESURE MONITOR?
The FDA product code for ELECTRONIC BLOOD PRESURE MONITOR 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.
Other records listing Shenzhen Pango Electronic Co., Ltd. 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: 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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