SCAN300FP / RETROPAN (VDC)— 510(k) K051664

Substantially Equivalent

Oy Ajat, Ltd.

FDA 510(k) clearance K051664 for SCAN300FP / RETROPAN (VDC), Substantially Equivalent on 2005-07-20. Applicant: Oy Ajat, Ltd.. Device class: 2.

Clearance details

Applicant: Oy Ajat, Ltd.
Product code: Code MUH
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2005-06-22
Decision date: 2005-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ormond Beach, FL, US

Download summary PDF View on FDA.gov ↗

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