FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000
K-Number: K952827 · 1996-11-14
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Device Summary
Frequently Asked Questions
What is the FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000?
FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 is a medical device that received FDA 510(k) clearance on 1996-11-14. The listed applicant is Sein Electronics Co., Ltd.. The 510(k) number is K952827.
When did FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 receive FDA 510(k) clearance?
FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 received FDA 510(k) clearance on 1996-11-14, under 510(k) number K952827.
Who is the listed applicant for FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000?
The FDA 510(k) record lists Sein Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000?
The FDA product code for FULL AUTO WRIST BLOOD PRESSURE METER MODEL SE-5000 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 Sein Electronics 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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