FDA 510(k) Applications Submitted by CHALGREN ENTERPRISES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960591 |
02/12/1996 |
RE-USABLE BIPOLAR CONCENTRIC NEEDLE(237-XXX-24,237-XXX-24STP, 237-XXX-24TP,237-XXX-24STP |
CHALGREN ENTERPRISES, INC. |
| K953354 |
07/17/1995 |
EMG DISC RECORDING ELECTRODE |
CHALGREN ENTERPRISES, INC. |
| K953356 |
07/17/1995 |
EMG RECORDING RING ELECTRODE |
CHALGREN ENTERPRISES, INC. |
| K953361 |
07/17/1995 |
EMG DISC RECORDING ELECTRODE |
CHALGREN ENTERPRISES, INC. |
| K982950 |
08/21/1998 |
FINE WIRE ELECTRODE MMODEL NUMBERS 221-14-730, 221-24-730, 221-14-550, 221-24-550 |
CHALGREN ENTERPRISES, INC. |
| K955335 |
11/20/1995 |
DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE |
CHALGREN ENTERPRISES, INC. |
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