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FDA 510(k), K000886, SPIROL EPIDURAL CATHETER
FDA 510(k), K000886, SPIROL EPIDURAL CATHETER
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510(K) Number: K000886
Device Name: SPIROL EPIDURAL CATHETER
Manufacturer: ABBOTT LABORATORIES
Device Classification Name: catheter, conduction, anesthetic
Regulation Number: 868.5120
Classification Product Code: BSO
Date Received: 03/20/2000
Decision Date: 10/05/2000
Regulation Medical Specialty: Anesthesiology
Device Name: SPIROL EPIDURAL CATHETER
Manufacturer: ABBOTT LABORATORIES
Device Classification Name: catheter, conduction, anesthetic
Regulation Number: 868.5120
Classification Product Code: BSO
Date Received: 03/20/2000
Decision Date: 10/05/2000
Regulation Medical Specialty: Anesthesiology
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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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