KWIKAP— 510(k) K772315

Substantially Equivalent

Den-Mat Corp.

FDA 510(k) clearance K772315 for KWIKAP, Substantially Equivalent on 1978-01-03. Applicant: Den-Mat Corp.. Device class: 1.

Clearance details

Applicant: Den-Mat Corp.
Product code: Code EMB
Device class: Class 1
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1977-12-19
Decision date: 1978-01-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Den-Mat Corp.

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K881918 — LIGHT-CURED ZIONOMER CEMENT1988-07-15
K875351 — DEN-MAT PORETCH (PORCELAIN ETCHANT)1988-03-18

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