RETISCAN, RETIPORT— 510(k) K023525

Substantially Equivalent

Roland Consult

FDA 510(k) clearance K023525 for RETISCAN, RETIPORT, Substantially Equivalent on 2004-03-26. Applicant: Roland Consult. Device class: 2.

Clearance details

Applicant: Roland Consult
Product code: Code GWE
Device class: Class 2
Regulation: 21 CFR 882.1890
Advisory panel: Neurology
Date received: 2002-10-21
Decision date: 2004-03-26
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Brandenburg, 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.