MICROJET CAVITY PREPARATION SYSTEM— 510(k) K964755

Name: FDA 510(k) clearance K964755
Creator: U.S. Food and Drug Administration
Published: 1997-09-11

Substantially Equivalent

Midwest Dental Products Corp.

FDA 510(k) clearance K964755 for MICROJET CAVITY PREPARATION SYSTEM, Substantially Equivalent on 1997-09-11. Applicant: Midwest Dental Products Corp.. Device class: 2.

Clearance details

Applicant: Midwest Dental Products Corp.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1996-11-27
Decision date: 1997-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Des Plaines, IL, US

Download summary PDF View on FDA.gov ↗

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