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FDA 510(k)

FLUOR-ETCH GEL ETCHANT

K-Number: K862695 · 1986-07-31

ApplicantTeledyne, Inc.
Decision Date1986-07-31
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLUOR-ETCH GEL ETCHANT is the device name listed in this FDA 510(k) record. The listed applicant is Teledyne, Inc.. It received FDA 510(k) clearance on 1986-07-31 under 510(k) number K862695. 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 FLUOR-ETCH GEL ETCHANT?

FLUOR-ETCH GEL ETCHANT is a medical device that received FDA 510(k) clearance on 1986-07-31. The listed applicant is Teledyne, Inc.. The 510(k) number is K862695.

When did FLUOR-ETCH GEL ETCHANT receive FDA 510(k) clearance?

FLUOR-ETCH GEL ETCHANT received FDA 510(k) clearance on 1986-07-31, under 510(k) number K862695.

Who is the listed applicant for FLUOR-ETCH GEL ETCHANT?

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

What is the FDA product code for FLUOR-ETCH GEL ETCHANT?

The FDA product code for FLUOR-ETCH GEL ETCHANT is EBC.

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Other records listing Teledyne, Inc. as applicant

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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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