DIAMOND PROBE/PERIO 2000 SYSTEM— 510(k) DEN980003

Name: FDA 510(k) clearance DEN980003
Creator: U.S. Food and Drug Administration
Published: 1998-07-17

Unknown

Diamond General Development Corp.

FDA 510(k) clearance DEN980003 for DIAMOND PROBE/PERIO 2000 SYSTEM, Unknown on 1998-07-17. Applicant: Diamond General Development Corp.. Device class: 2.

Clearance details

Applicant: Diamond General Development Corp.
Product code: Code MVH
Device class: Class 2
Regulation: 21 CFR 872.1870
Advisory panel: Dental
Date received: 1998-05-18
Decision date: 1998-07-17
Decision: Unknown
Clearance type: Post-NSE
Location: Ann Arbor, MI, US

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