L-LINEX-RAY FLUORESCENCE— 510(k) K911749

Name: FDA 510(k) clearance K911749
Creator: U.S. Food and Drug Administration
Published: 1991-08-20

Substantially Equivalent

Montifore Medical Center

FDA 510(k) clearance K911749 for L-LINEX-RAY FLUORESCENCE, Substantially Equivalent on 1991-08-20. Applicant: Montifore Medical Center. Device class: 2.

Clearance details

Applicant: Montifore Medical Center
Product code: Code JAO
Device class: Class 2
Regulation: 21 CFR 892.1220
Advisory panel: Radiology
Date received: 1991-04-18
Decision date: 1991-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bronx, NY, US

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