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FDA 510(k), K082626, PAM 3000
FDA 510(k), K082626, PAM 3000
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$149.00 USD
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$149.00 USD
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510(K) Number: K082626
Device Name: PAM 3000
Manufacturer: WIRELESS 2000 RF & UWB TECHNOLOGIES LTD.
Device Classification Name: monitor, cardiac (incl. cardiotachometer & rate alarm)
Regulation Number: 870.2300
Classification Product Code: DRT
Date Received: 09/09/2008
Decision Date: 01/16/2009
Regulation Medical Specialty: Cardiovascular
Device Name: PAM 3000
Manufacturer: WIRELESS 2000 RF & UWB TECHNOLOGIES LTD.
Device Classification Name: monitor, cardiac (incl. cardiotachometer & rate alarm)
Regulation Number: 870.2300
Classification Product Code: DRT
Date Received: 09/09/2008
Decision Date: 01/16/2009
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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