FDA 510(k) Application Details - K233398

Device Classification Name	Unit, Phacofragmentation   More FDA Info for this Device
510(K) Number	K233398
Device Name	Unit, Phacofragmentation
Applicant	Oertli Instrumente AG Hafnerwiesenstrasse 4 Berneck 9442 CH Other 510(k) Applications for this Company
Contact	Marianne Kesseli Other 510(k) Applications for this Contact
Regulation Number	886.4670   More FDA Info for this Regulation Number
Classification Product Code	HQC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/03/2023
Decision Date	06/27/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review