FDA 510(k), K930622, AMPLATZ GUIDEWIRES

FDA 510(k), K930622, AMPLATZ GUIDEWIRES

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510(K) Number: K930622
Device Name: AMPLATZ GUIDEWIRES
Manufacturer:
Device Classification Name: Wire, Guide, Catheter
Regulation Number: 870.1330
Classification Product Code: DQX
Date Received: 02/08/1993
Decision Date: 04/29/1993
Regulation Medical Specialty: Cardiovascular
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