BRAINSCAN BRACHYTHERAPY MODULE— 510(k) K920880

Substantially Equivalent

Brainlab

FDA 510(k) clearance K920880 for BRAINSCAN BRACHYTHERAPY MODULE, Substantially Equivalent on 1992-12-30. Applicant: Brainlab. Device class: 2.

Clearance details

Applicant: Brainlab
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 1992-02-26
Decision date: 1992-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Germany, DE

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.