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FDA 510(k)

BIOZ SYSTEM & BIOZ PORTABLE

K-Number: K972320 · 1997-09-11

ApplicantCardiodynamics International Corp.
Decision Date1997-09-11
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIOZ SYSTEM & BIOZ PORTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Cardiodynamics International Corp.. It received FDA 510(k) clearance on 1997-09-11 under 510(k) number K972320. 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 BIOZ SYSTEM & BIOZ PORTABLE?

BIOZ SYSTEM & BIOZ PORTABLE is a medical device that received FDA 510(k) clearance on 1997-09-11. The listed applicant is Cardiodynamics International Corp.. The 510(k) number is K972320.

When did BIOZ SYSTEM & BIOZ PORTABLE receive FDA 510(k) clearance?

BIOZ SYSTEM & BIOZ PORTABLE received FDA 510(k) clearance on 1997-09-11, under 510(k) number K972320.

Who is the listed applicant for BIOZ SYSTEM & BIOZ PORTABLE?

The FDA 510(k) record lists Cardiodynamics International Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOZ SYSTEM & BIOZ PORTABLE?

The FDA product code for BIOZ SYSTEM & BIOZ PORTABLE is DSB.

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Other records listing Cardiodynamics International 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.

K090602CARDIODYNAMICS BIOZ RX, MODEL 7101-SYSK070156BIOZ DX HEMODYNAMIC MONITOR WITH PHILIPS 12-LEAD ECG, MODEL 5100K051228BIOZDX HEMODYNAMIC MONITOR AND 12-LEAD ECGK041294BIOZDX HEMODYNAMIC MONITORK011439MODIFICATION TO BIOZ.COM HEMODYNAMIC MONITORK011797BIOZTECT SENSOR AND BIOZTECT CABLE

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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

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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