DENTAL INSTRUMENTS SCALER— 510(k) K931330

Name: FDA 510(k) clearance K931330
Creator: U.S. Food and Drug Administration
Published: 1994-01-26

Substantially Equivalent

Minnesota Prophy Power, Inc.

FDA 510(k) clearance K931330 for DENTAL INSTRUMENTS SCALER, Substantially Equivalent on 1994-01-26. Applicant: Minnesota Prophy Power, Inc.. Device class: 1.

Clearance details

Applicant: Minnesota Prophy Power, Inc.
Product code: Code EMN
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1993-03-16
Decision date: 1994-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeville, MN, US

Download summary PDF View on FDA.gov ↗

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K931329 — DENTAL INSTRUMENTS CURETTE PERIODONTAL1994-01-27

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