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FDA 510(k)

GLY-ETCH

K-Number: K961190 · 1996-04-23

ApplicantCentrix, Inc.
Decision Date1996-04-23
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GLY-ETCH is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 1996-04-23 under 510(k) number K961190. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLY-ETCH?

GLY-ETCH is a medical device that received FDA 510(k) clearance on 1996-04-23. The listed applicant is Centrix, Inc.. The 510(k) number is K961190.

When did GLY-ETCH receive FDA 510(k) clearance?

GLY-ETCH received FDA 510(k) clearance on 1996-04-23, under 510(k) number K961190.

Who is the listed applicant for GLY-ETCH?

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

What is the FDA product code for GLY-ETCH?

The FDA product code for GLY-ETCH is EBC.

Other records listing Centrix, Inc. as applicant

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Related Devices (Code: EBC)

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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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