DEN-MAT PORETCH (PORCELAIN ETCHANT)— 510(k) K875351

Name: FDA 510(k) clearance K875351
Creator: U.S. Food and Drug Administration
Published: 1988-03-18

Substantially Equivalent

Den-Mat Corp.

FDA 510(k) clearance K875351 for DEN-MAT PORETCH (PORCELAIN ETCHANT), Substantially Equivalent on 1988-03-18. Applicant: Den-Mat Corp.. Device class: 2.

Clearance details

Applicant: Den-Mat Corp.
Product code: Code ELL
Device class: Class 2
Regulation: 21 CFR 872.3920
Advisory panel: Dental
Date received: 1987-12-31
Decision date: 1988-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Maria, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.