FDA 510(k), K950889, ADEL 5000
FDA 510(k), K950889, ADEL 5000
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510(K) Number: K950889
Device Name: ADEL 5000
Manufacturer: STRYKER CORP.
Device Classification Name: table, obstetrical, ac-powered (and accessories)
Regulation Number: 884.4900
Classification Product Code: HDD
Date Received: 02/28/1995
Decision Date: 10/16/1995
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: ADEL 5000
Manufacturer: STRYKER CORP.
Device Classification Name: table, obstetrical, ac-powered (and accessories)
Regulation Number: 884.4900
Classification Product Code: HDD
Date Received: 02/28/1995
Decision Date: 10/16/1995
Regulation Medical Specialty: Obstetrics/Gynecology
- 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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