GE PHOTON ENERGY RECOVERY (PER) OPTION— 510(k) K023932

Name: FDA 510(k) clearance K023932
Creator: U.S. Food and Drug Administration
Published: 2002-12-11

Substantially Equivalent

Ge Medical Systems F.I. Haifa

FDA 510(k) clearance K023932 for GE PHOTON ENERGY RECOVERY (PER) OPTION, Substantially Equivalent on 2002-12-11. Applicant: Ge Medical Systems F.I. Haifa. Device class: 2.

Clearance details

Applicant: Ge Medical Systems F.I. Haifa
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 2002-11-26
Decision date: 2002-12-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tirat Hacarmel, IL

Download summary PDF View on FDA.gov ↗

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