NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050
K-Number: K850477 · 1985-04-29
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Device Summary
Frequently Asked Questions
What is the NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050?
NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050 is a medical device that received FDA 510(k) clearance on 1985-04-29. The listed applicant is Unisonic Products Corp.. The 510(k) number is K850477.
When did NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050 receive FDA 510(k) clearance?
NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050 received FDA 510(k) clearance on 1985-04-29, under 510(k) number K850477.
Who is the listed applicant for NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050?
The FDA 510(k) record lists Unisonic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050?
The FDA product code for NONINVASIVE ELECTRONIC DIGITAL BP MONITOR EBM-2050 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 Unisonic Products Corp. 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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