RETISCAN, RETIPORT


Device Classification Name

stimulator, photic, evoked response

510(k) Number K023525
Device Name RETISCAN, RETIPORT
Original Applicant
ROLAND CONSULT
friedrich-franz-strasse 19
brandenburg, 

DE

d 14770

Original Contact matthias mai
Regulation Number 882.1890
Classification Product Code
GWE  
Date Received 10/21/2002
Decision Date 03/26/2004
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No