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FDA 510(k)

OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630

K-Number: K911722 · 1992-01-22

ApplicantCas Medical Systems, Inc.
Decision Date1992-01-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630 is the device name listed in this FDA 510(k) record. The listed applicant is Cas Medical Systems, Inc.. It received FDA 510(k) clearance on 1992-01-22 under 510(k) number K911722. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630?

OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630 is a medical device that received FDA 510(k) clearance on 1992-01-22. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K911722.

When did OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630 receive FDA 510(k) clearance?

OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630 received FDA 510(k) clearance on 1992-01-22, under 510(k) number K911722.

Who is the listed applicant for OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630?

The FDA 510(k) record lists Cas Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630?

The FDA product code for OSCILLOMATE (TM) BLOOD PRESSURE MONITOR-MODEL 1630 is DXN.

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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.

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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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