PELICAN BAY KEL-COR CEPHALOMETRIC SYS.— 510(k) K791916

Name: FDA 510(k) clearance K791916
Creator: U.S. Food and Drug Administration
Published: 1979-11-05

Substantially Equivalent

Pelican Bay Kel-Cor

FDA 510(k) clearance K791916 for PELICAN BAY KEL-COR CEPHALOMETRIC SYS., Substantially Equivalent on 1979-11-05. Applicant: Pelican Bay Kel-Cor. Device class: 1.

Clearance details

Applicant: Pelican Bay Kel-Cor
Product code: Code IXY
Device class: Class 1
Regulation: 21 CFR 892.1880
Advisory panel: Radiology
Date received: 1979-09-25
Decision date: 1979-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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