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FDA 510(k)

ENDO-GLIDE

K-Number: K013701 · 2002-02-04

ApplicantSonotech, Inc.
Decision Date2002-02-04
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDO-GLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Sonotech, Inc.. It received FDA 510(k) clearance on 2002-02-04 under 510(k) number K013701. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-GLIDE?

ENDO-GLIDE is a medical device that received FDA 510(k) clearance on 2002-02-04. The listed applicant is Sonotech, Inc.. The 510(k) number is K013701.

When did ENDO-GLIDE receive FDA 510(k) clearance?

ENDO-GLIDE received FDA 510(k) clearance on 2002-02-04, under 510(k) number K013701.

Who is the listed applicant for ENDO-GLIDE?

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

What is the FDA product code for ENDO-GLIDE?

The FDA product code for ENDO-GLIDE is GCJ.

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Related Devices (Code: GCJ)

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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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