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FDA 510(k)

KINESIA

K-Number: K063872 · 2007-04-06

ApplicantCleveland Medical Devices, Inc.
Decision Date2007-04-06
Product CodeGYD
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

KINESIA is the device name listed in this FDA 510(k) record. The listed applicant is Cleveland Medical Devices, Inc.. It received FDA 510(k) clearance on 2007-04-06 under 510(k) number K063872. The device is classified under product code GYD. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINESIA?

KINESIA is a medical device that received FDA 510(k) clearance on 2007-04-06. The listed applicant is Cleveland Medical Devices, Inc.. The 510(k) number is K063872.

When did KINESIA receive FDA 510(k) clearance?

KINESIA received FDA 510(k) clearance on 2007-04-06, under 510(k) number K063872.

Who is the listed applicant for KINESIA?

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

What is the FDA product code for KINESIA?

The FDA product code for KINESIA is GYD.

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Other records listing Cleveland Medical Devices, 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.

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Related Devices (Code: GYD)

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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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