FDA 510(k), K130210, MEDELA THOPAZ
FDA 510(k), K130210, MEDELA THOPAZ
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510(K) Number: K130210
Device Name: MEDELA THOPAZ
Manufacturer: MEDELA AG
Device Classification Name: pump, portable, aspiration (manual or powered)
Regulation Number: 878.4780
Classification Product Code: BTA
Date Received: 01/29/2013
Decision Date: 03/15/2013
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MEDELA THOPAZ
Manufacturer: MEDELA AG
Device Classification Name: pump, portable, aspiration (manual or powered)
Regulation Number: 878.4780
Classification Product Code: BTA
Date Received: 01/29/2013
Decision Date: 03/15/2013
Regulation Medical Specialty: General & Plastic Surgery