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FDA 510(k)

CHEETAH I.V.D.S., MODEL 2002P

K-Number: K023370 · 2002-12-24

ApplicantCheetah Medical, Inc.
Decision Date2002-12-24
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHEETAH I.V.D.S., MODEL 2002P 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 2002-12-24 under 510(k) number K023370. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHEETAH I.V.D.S., MODEL 2002P?

CHEETAH I.V.D.S., MODEL 2002P is a medical device that received FDA 510(k) clearance on 2002-12-24. The listed applicant is Cheetah Medical, Inc.. The 510(k) number is K023370.

When did CHEETAH I.V.D.S., MODEL 2002P receive FDA 510(k) clearance?

CHEETAH I.V.D.S., MODEL 2002P received FDA 510(k) clearance on 2002-12-24, under 510(k) number K023370.

Who is the listed applicant for CHEETAH I.V.D.S., MODEL 2002P?

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 CHEETAH I.V.D.S., MODEL 2002P?

The FDA product code for CHEETAH I.V.D.S., MODEL 2002P is DQK.

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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 ACTIVEK042144NICOM

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Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, 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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