PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT— 510(k) K965072

Name: FDA 510(k) clearance K965072
Creator: U.S. Food and Drug Administration
Published: 1997-01-27

Substantially Equivalent

Kaycor Intl., Ltd.

FDA 510(k) clearance K965072 for PANOURA ULTRA PAN AND PANOURA ULTRA PAN/CEPH PANORAMIC/CEPHALOMETRIC X-RAY UNIT, Substantially Equivalent on 1997-01-27. Applicant: Kaycor Intl., Ltd.. Device class: 2.

Clearance details

Applicant: Kaycor Intl., Ltd.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 1996-12-19
Decision date: 1997-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Northbrook, IL, US

Download summary PDF View on FDA.gov ↗

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