Carl Zeiss Meditec, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CLARUS (700), CIRRUS™ HD-OCT Model 6000, VISULAS yag
29
Total
29
Cleared
0
Denied
FDA 510(k) Regulatory Record - Carl Zeiss Meditec, Inc. General & Plastic Surgery ✕
1 devices