DENTAL INSTRUMENTS CURETTE PERIODONTAL— 510(k) K931329

Name: FDA 510(k) clearance K931329
Creator: U.S. Food and Drug Administration
Published: 1994-01-27

Substantially Equivalent

Minnesota Prophy Power, Inc.

FDA 510(k) clearance K931329 for DENTAL INSTRUMENTS CURETTE PERIODONTAL, Substantially Equivalent on 1994-01-27. Applicant: Minnesota Prophy Power, Inc.. Device class: 1.

Clearance details

Applicant: Minnesota Prophy Power, Inc.
Product code: Code EMS
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1993-03-16
Decision date: 1994-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lakeville, MN, US

Download summary PDF View on FDA.gov ↗

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K931330 — DENTAL INSTRUMENTS SCALER1994-01-26

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