FDA 510(k), K970418, PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
FDA 510(k), K970418, PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
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510(K) Number: K970418
Device Name: PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
Manufacturer:
Device Classification Name: Electrode, Depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 02/04/1997
Decision Date: 04/29/1997
Regulation Medical Specialty: Neurology
Device Name: PMT ACCESSORY DEPTHALON ELECTRODE ANCHOR BOLT (2103-23-XX)
Manufacturer:
Device Classification Name: Electrode, Depth
Regulation Number: 882.1330
Classification Product Code: GZL
Date Received: 02/04/1997
Decision Date: 04/29/1997
Regulation Medical Specialty: Neurology