FDA 510(k) Applications Submitted by STOELTING CO.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K952797 | 06/19/1995 | AT53 DUAL CHANNEL EMG | STOELTING CO. |
| K965006 | 12/16/1996 | AT 62 EEG (A.K.A THE A;PHA-THETA TRAINER) | STOELTING CO. |
| K012011 | 06/28/2001 | MODIFICATION TO A620 EEG | STOELTING CO. |
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