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FDA 510(k), K032519, ENDO PAT 2000
FDA 510(k), K032519, ENDO PAT 2000
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510(K) Number: K032519
Device Name: ENDO PAT 2000
Manufacturer: DORIT WINITZ
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: DQK
Classification Product Code: 08/15/2003
Date Received: 11/12/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: ENDO PAT 2000
Manufacturer: DORIT WINITZ
Device Classification Name: Computer, Diagnostic, Programmable
Regulation Number: DQK
Classification Product Code: 08/15/2003
Date Received: 11/12/2003
Decision Date: Substantially Equivalent (SESE)
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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