FDA 510(k)

IPS CERAMIC ETCHING GEL

K-Number: K923926 · 1992-10-27

Decision Date1992-10-27

Product CodeELL

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

IPS CERAMIC ETCHING GEL is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar North America, Inc.. It received FDA 510(k) clearance on 1992-10-27 under 510(k) number K923926. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPS CERAMIC ETCHING GEL?

IPS CERAMIC ETCHING GEL is a medical device that received FDA 510(k) clearance on 1992-10-27. The listed applicant is Ivoclar North America, Inc.. The 510(k) number is K923926.

When did IPS CERAMIC ETCHING GEL receive FDA 510(k) clearance?

IPS CERAMIC ETCHING GEL received FDA 510(k) clearance on 1992-10-27, under 510(k) number K923926.

Who is the listed applicant for IPS CERAMIC ETCHING GEL?

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

What is the FDA product code for IPS CERAMIC ETCHING GEL?

The FDA product code for IPS CERAMIC ETCHING GEL is ELL.

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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.