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FDA 510(k)

CLEARJET

K-Number: K101094 · 2010-05-17

ApplicantEasyglide , Ltd.
Decision Date2010-05-17
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLEARJET is the device name listed in this FDA 510(k) record. The listed applicant is Easyglide , Ltd.. It received FDA 510(k) clearance on 2010-05-17 under 510(k) number K101094. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARJET?

CLEARJET is a medical device that received FDA 510(k) clearance on 2010-05-17. The listed applicant is Easyglide , Ltd.. The 510(k) number is K101094.

When did CLEARJET receive FDA 510(k) clearance?

CLEARJET received FDA 510(k) clearance on 2010-05-17, under 510(k) number K101094.

Who is the listed applicant for CLEARJET?

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

What is the FDA product code for CLEARJET?

The FDA product code for CLEARJET is ODC.

Related Clinical Trials

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Other records listing Easyglide , Ltd. 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.

K113050CLEARPATH LOWER GIK113166CLEARPATH UPPER GIK093779CLEARPATH UGIK091305CLEARPATH

Related Devices (Code: ODC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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