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FDA 510(k)

C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS

K-Number: K041434 · 2004-08-06

ApplicantAnalogic Corp.
Decision Date2004-08-06
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corp.. It received FDA 510(k) clearance on 2004-08-06 under 510(k) number K041434. 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 C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS?

C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS is a medical device that received FDA 510(k) clearance on 2004-08-06. The listed applicant is Analogic Corp.. The 510(k) number is K041434.

When did C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS receive FDA 510(k) clearance?

C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS received FDA 510(k) clearance on 2004-08-06, under 510(k) number K041434.

Who is the listed applicant for C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS?

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

What is the FDA product code for C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS?

The FDA product code for C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS is DSB.

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Other records listing Analogic 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.

K071430SYNERAD OMNI, MODELS AN6255 AND AN6265K052447SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600K050919LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423PK043025SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250K041376C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925AK040995SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150

View all 32 devices →

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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