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FDA 510(k)

SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH

K-Number: K014299 · 2002-01-30

ApplicantSorba Medical Systems, Inc.
Decision Date2002-01-30
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Sorba Medical Systems, Inc.. It received FDA 510(k) clearance on 2002-01-30 under 510(k) number K014299. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH?

SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH is a medical device that received FDA 510(k) clearance on 2002-01-30. The listed applicant is Sorba Medical Systems, Inc.. The 510(k) number is K014299.

When did SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH receive FDA 510(k) clearance?

SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH received FDA 510(k) clearance on 2002-01-30, under 510(k) number K014299.

Who is the listed applicant for SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH?

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

What is the FDA product code for SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH?

The FDA product code for SORBA STEORRA NON-INVASIVE IMPEDANCE CARDIOGRAPH is DSB.

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Other records listing Sorba Medical Systems, Inc. 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.

K950389SORBA MODEL CIC-1000 NON-INVASIVE HEMODYNAMIC MONITORK901926SORBA MODEL CIC-1000 W/NEW ELECTRODESK895017SORBA MODEL CIC-1000, COMP. IMPEDANCE CARDIOGRAPH

Related Devices (Code: DSB)

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.

K260224MySOZO Software version 6.1.0.1 (SW version 6.1.0.1)ImpediMed LimitedK250634BCM2-Body Composition MonitorFresenius Medical Care Renal Therapies Group, LLCK243727Re:BalansMode Sensors ASK250922Edema Guard Monitor (EGM) CardioSet-001Cardioset Medical , Ltd.K232089SOZO ProImpediMed LimitedK223217Zynex Monitoring System, Model CM-1600Zynex Medical, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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