MICRORUPTER V


Device Classification Name

laser, neodymium:yag, ophthalmic for posterior capsulotomy and cutting pupilla

510(k) Number K023045
Device Name MICRORUPTER V
Original Applicant
MERIDIAN AG
bierigutstrasse 7
thun, bern, 

CH

3608

Original Contact kurt frey
Regulation Number 886.4392
Classification Product Code
LXS  
Date Received 09/12/2002
Decision Date 09/26/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Ophthalmic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party Yes

Combination Product

No