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FDA 510(k)

NICOM

K-Number: K042144 · 2004-11-12

ApplicantCheetah Medical, Inc.
Decision Date2004-11-12
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NICOM is the device name listed in this FDA 510(k) record. The listed applicant is Cheetah Medical, Inc.. It received FDA 510(k) clearance on 2004-11-12 under 510(k) number K042144. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICOM?

NICOM is a medical device that received FDA 510(k) clearance on 2004-11-12. The listed applicant is Cheetah Medical, Inc.. The 510(k) number is K042144.

When did NICOM receive FDA 510(k) clearance?

NICOM received FDA 510(k) clearance on 2004-11-12, under 510(k) number K042144.

Who is the listed applicant for NICOM?

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

What is the FDA product code for NICOM?

The FDA product code for NICOM is DXG.

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Other records listing Cheetah Medical, 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.

K103166CHEETAH RELIANTK101487CHEETAH NICOM SYSTEMK083093CHEETAH RELIANTK071631NICOM ELECTRODESK072662CHEETAH RELIANT, CHEETAH ACTIVEK023370CHEETAH I.V.D.S., MODEL 2002P

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Related Devices (Code: DXG)

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.

K253092Argos Infinity (Rev. 1.0)Retia Medical Systems, Inc.K251275VitalStream ART Connect; VitalStream-HemoCaretaker MedicalK232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSIcu MedicalK212529Hypotension Decision Assist Model HDA-OR2Directed Systems, Ltd.K192169PulsioFlex Monitoring System with ProAQT SensorPulsion Medical Systems SEK193179EV1000 Clinical PlatformEdwards Lifesciences, LLC

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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