Bisco Porcelain Etching Gel

FDA 510(k) K926238 · Bisco, Inc.

Substantially Equivalent

510(k) numberK926238

Submission

Device name
Bisco Porcelain Etching Gel
Applicant
Bisco, Inc.
Itasca, IL, US
Received
December 11, 1992
Decision date
March 31, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EIH – Powder, Porcelain
Device class
Class II (moderate risk)
Regulation
21 CFR 872.6660
Specialty
Dental

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Questions and answers

When was Bisco Porcelain Etching Gel cleared by the FDA?

Bisco Porcelain Etching Gel (K926238) received a 510(k) decision of Substantially Equivalent on March 31, 1993, 110 days after the submission was received.

What is the product code of K926238?

The FDA product code is EIH – Powder, Porcelain, a Class II (moderate risk) device regulated under 21 CFR 872.6660.