ANEROID TYPE BLOOD PRESSURE KIT
K-Number: K780715 · 1978-07-17
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Device Summary
Frequently Asked Questions
What is the ANEROID TYPE BLOOD PRESSURE KIT?
ANEROID TYPE BLOOD PRESSURE KIT is a medical device that received FDA 510(k) clearance on 1978-07-17. The listed applicant is Mars Metal Co., Ltd.. The 510(k) number is K780715.
When did ANEROID TYPE BLOOD PRESSURE KIT receive FDA 510(k) clearance?
ANEROID TYPE BLOOD PRESSURE KIT received FDA 510(k) clearance on 1978-07-17, under 510(k) number K780715.
Who is the listed applicant for ANEROID TYPE BLOOD PRESSURE KIT?
The FDA 510(k) record lists Mars Metal Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANEROID TYPE BLOOD PRESSURE KIT?
The FDA product code for ANEROID TYPE BLOOD PRESSURE KIT 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 Mars Metal 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: 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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