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FDA 510(k)

HORIZON REGULAR ETCHING GEL

K-Number: K904199 · 1990-12-05

ApplicantHorizon Chemical Co.
Decision Date1990-12-05
Product CodeEJR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HORIZON REGULAR ETCHING GEL is the device name listed in this FDA 510(k) record. The listed applicant is Horizon Chemical Co.. It received FDA 510(k) clearance on 1990-12-05 under 510(k) number K904199. The device is classified under product code EJR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON REGULAR ETCHING GEL?

HORIZON REGULAR ETCHING GEL is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Horizon Chemical Co.. The 510(k) number is K904199.

When did HORIZON REGULAR ETCHING GEL receive FDA 510(k) clearance?

HORIZON REGULAR ETCHING GEL received FDA 510(k) clearance on 1990-12-05, under 510(k) number K904199.

Who is the listed applicant for HORIZON REGULAR ETCHING GEL?

The FDA 510(k) record lists Horizon Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HORIZON REGULAR ETCHING GEL?

The FDA product code for HORIZON REGULAR ETCHING GEL is EJR.

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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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