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FDA 510(k)

CHEETAH RELIANT

K-Number: K083093 · 2008-12-15

ApplicantCheetah Medical, Inc.
Decision Date2008-12-15
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHEETAH RELIANT 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 2008-12-15 under 510(k) number K083093. 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 CHEETAH RELIANT?

CHEETAH RELIANT is a medical device that received FDA 510(k) clearance on 2008-12-15. The listed applicant is Cheetah Medical, Inc.. The 510(k) number is K083093.

When did CHEETAH RELIANT receive FDA 510(k) clearance?

CHEETAH RELIANT received FDA 510(k) clearance on 2008-12-15, under 510(k) number K083093.

Who is the listed applicant for CHEETAH RELIANT?

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 RELIANT?

The FDA product code for CHEETAH RELIANT is DSB.

Related Clinical Trials

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.

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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 SYSTEMK071631NICOM ELECTRODESK072662CHEETAH RELIANT, CHEETAH ACTIVEK042144NICOMK023370CHEETAH I.V.D.S., MODEL 2002P

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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.

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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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