FDA 510(k) Applications for Medical Device Product Code "DRR"
(Amplifier And Signal Conditioner, Biopotential)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K022660 | BIOCHECK, INC. | BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117 | 12/19/2002 |
| K971570 | QUINTON ELECTROPHYSIOLOGY CORP. | EPXPRESS SYSTEM (TIMBERWOLF REVISION) /000391 | 12/29/1997 |
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