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FDA 510(k)

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR

K-Number: K972020 · 1998-05-05

ApplicantCas Medical Systems, Inc.
Decision Date1998-05-05
Product CodeDXW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR 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 1998-05-05 under 510(k) number K972020. The device is classified under product code DXW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR?

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1998-05-05. The listed applicant is Cas Medical Systems, Inc.. The 510(k) number is K972020.

When did OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR receive FDA 510(k) clearance?

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1998-05-05, under 510(k) number K972020.

Who is the listed applicant for OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR?

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 NON-INVASIVE BLOOD PRESSURE MONITOR?

The FDA product code for OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR is DXW.

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Other records listing Cas Medical Systems, Inc. as applicant

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Related Devices (Code: DXW)

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.

K955887NEWMED ABP-LITENewmed Corp.K802830MILLAR MIKRO-TIP CATHETER PHONOTRANSMillar Instruments, Inc.K800222MODEL 412 ELECTROFLUIDIC MANOMETERMed-Tek Corp.K800179INFRASONDE AUTO/INFLATOR ELEC. VIBRATORSphygmetrics, Inc.

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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