FDA 510(k), K063844, REPROCESSED HEART STABILIZERS AND POSITIONERS

FDA 510(k), K063844, REPROCESSED HEART STABILIZERS AND POSITIONERS

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510(K) Number: K063844
Device Name: REPROCESSED HEART STABILIZERS AND POSITIONERS
Manufacturer:
Device Classification Name: Stabilizer, Heart, Non-Compression, Reprocessed
Regulation Number: 870.4500
Classification Product Code: NQG
Date Received: 12/26/2006
Decision Date: 03/15/2007
Regulation Medical Specialty: Cardiovascular
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