SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR
K-Number: K852421 · 1986-02-26
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Device Summary
Frequently Asked Questions
What is the SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR?
SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1986-02-26. The listed applicant is Nbs Medical, Inc.. The 510(k) number is K852421.
When did SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?
SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1986-02-26, under 510(k) number K852421.
Who is the listed applicant for SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR?
The FDA 510(k) record lists Nbs Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SENTRY II NONINDWELLING BLOOD PRESSURE MONITOR?
The FDA product code for SENTRY II NONINDWELLING BLOOD PRESSURE 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.
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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