BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE
K-Number: K850893 · 1985-05-16
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Device Summary
Frequently Asked Questions
What is the BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?
BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE is a medical device that received FDA 510(k) clearance on 1985-05-16. The listed applicant is Sun Dance Technology, Inc.. The 510(k) number is K850893.
When did BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE receive FDA 510(k) clearance?
BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE received FDA 510(k) clearance on 1985-05-16, under 510(k) number K850893.
Who is the listed applicant for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?
The FDA 510(k) record lists Sun Dance Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE?
The FDA product code for BP/CLINIC SYS MEASUREMENT, BP NON-INVASIVE 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.
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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