RM BOND, MODEL J032— 510(k) K072830

Name: FDA 510(k) clearance K072830
Creator: U.S. Food and Drug Administration
Published: 2007-12-04

Substantially Equivalent

Pentron Clinical Technologies

FDA 510(k) clearance K072830 for RM BOND, MODEL J032, Substantially Equivalent on 2007-12-04. Applicant: Pentron Clinical Technologies. Device class: 2.

Clearance details

Applicant: Pentron Clinical Technologies
Product code: Code DYH
Device class: Class 2
Regulation: 21 CFR 872.3750
Advisory panel: Dental
Date received: 2007-10-03
Decision date: 2007-12-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wallingford, CT, US

Download summary PDF View on FDA.gov ↗

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