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FDA 510(k)

Y-GLIDE

K-Number: K072745 · 2008-01-04

ApplicantThomas Medical Products, Inc.
Decision Date2008-01-04
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Y-GLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Medical Products, Inc.. It received FDA 510(k) clearance on 2008-01-04 under 510(k) number K072745. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Y-GLIDE?

Y-GLIDE is a medical device that received FDA 510(k) clearance on 2008-01-04. The listed applicant is Thomas Medical Products, Inc.. The 510(k) number is K072745.

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

Y-GLIDE received FDA 510(k) clearance on 2008-01-04, under 510(k) number K072745.

Who is the listed applicant for Y-GLIDE?

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

What is the FDA product code for Y-GLIDE?

The FDA product code for Y-GLIDE is DTL.

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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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