ISOSEEDS I-125— 510(k) K021343

Name: FDA 510(k) clearance K021343
Creator: U.S. Food and Drug Administration
Published: 2002-05-20

Substantially Equivalent

Bebig Isotopen-Und Medizintechnik GmbH

FDA 510(k) clearance K021343 for ISOSEEDS I-125, Substantially Equivalent on 2002-05-20. Applicant: Bebig Isotopen-Und Medizintechnik GmbH. Device class: 2.

Clearance details

Applicant: Bebig Isotopen-Und Medizintechnik GmbH
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 2002-04-29
Decision date: 2002-05-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Berlin, DE

Download summary PDF View on FDA.gov ↗

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