FDA 510(k) Application Details - K213527

Device Classification Name	System, Image Management, Ophthalmic   More FDA Info for this Device
510(K) Number	K213527
Device Name	System, Image Management, Ophthalmic
Applicant	Carl Zeiss Meditec AG Goeschwitzer Strasse 51-52 Jena 07745 DE Other 510(k) Applications for this Company
Contact	Stefan Wimmer Other 510(k) Applications for this Contact
Regulation Number	892.2050   More FDA Info for this Regulation Number
Classification Product Code	NFJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/04/2021
Decision Date	08/15/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	RA - Radiology
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review