Heine Optotechnik GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: HEINE BETA 200, HEINE BETA 200 S, HEINE K 180, HEINE SIGMA 250 & HEINE SIGMA 250 M2, HEINE MINI 3000(R) OPHTHALMOSCOPE
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Heine Optotechnik GmbH & Co. KG Cardiovascular ✕
1 devices