Medical Device Manufacturer · US , Gilroy , CA

Chalgren Enterprises, Inc. - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1989

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

Chalgren Enterprises, Inc. has 21 FDA 510(k) cleared neurology devices. Based in Gilroy, US.

Historical record: 21 cleared submissions from 1989 to 1999.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Chalgren Enterprises, Inc.

21 devices
1-12 of 21
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