Chalgren Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chalgren Enterprises, Inc. - FDA 510(k) Cleared Devices
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
Cleared
Jun 22, 1999
FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550,...
Neurology
305d
Cleared
Jun 13, 1996
RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP,...
Neurology
122d
Cleared
Jan 29, 1996
DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE
Neurology
70d
Cleared
Jan 22, 1996
EMG DISC RECORDING ELECTRODE
Neurology
189d
Cleared
Jan 22, 1996
EMG RECORDING RING ELECTRODE
Neurology
189d
Cleared
Jan 22, 1996
EMG DISC RECORDING ELECTRODE
Neurology
189d
Cleared
Dec 06, 1995
EMG DISC RECORDING ELECTRODE WITH PIN
Neurology
177d
Cleared
Dec 06, 1995
EMG DISC RECORDING ELECTRODE WITH PIN
Neurology
166d
Cleared
Oct 31, 1995
RE-USABLE MONOPOLAR NEEDLE
Neurology
75d
Cleared
Oct 31, 1995
RE-USABLE CONCENTRIC NEEDLE
Neurology
75d
Cleared
Oct 06, 1995
22MM STAINLESS STEEL DISC ELECTRODE, WITH PIN
Neurology
88d
Cleared
Oct 06, 1995
32MM NICKEL PLATED DISC ELECTRODE
Neurology
88d