Chalgren Enterprises, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550, RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP, DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Chalgren Enterprises, Inc. Ophthalmic ✕
1 devices