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FDA 510(k)

CHEETAH NICOM SYSTEM

K-Number: K101487 · 2010-07-02

ApplicantCheetah Medical, Inc.
Decision Date2010-07-02
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHEETAH NICOM SYSTEM 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 2010-07-02 under 510(k) number K101487. 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 CHEETAH NICOM SYSTEM?

CHEETAH NICOM SYSTEM is a medical device that received FDA 510(k) clearance on 2010-07-02. The listed applicant is Cheetah Medical, Inc.. The 510(k) number is K101487.

When did CHEETAH NICOM SYSTEM receive FDA 510(k) clearance?

CHEETAH NICOM SYSTEM received FDA 510(k) clearance on 2010-07-02, under 510(k) number K101487.

Who is the listed applicant for CHEETAH NICOM SYSTEM?

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 NICOM SYSTEM?

The FDA product code for CHEETAH NICOM SYSTEM 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 RELIANTK083093CHEETAH RELIANTK071631NICOM ELECTRODESK072662CHEETAH RELIANT, CHEETAH ACTIVEK042144NICOMK023370CHEETAH I.V.D.S., MODEL 2002P

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Related Devices (Code: DXG)

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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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