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FDA 510(k), K021896, HSA-SOLUTION, MODEL 10034/10064
FDA 510(k), K021896, HSA-SOLUTION, MODEL 10034/10064
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510(K) Number: K021896
Device Name: HSA-SOLUTION, MODEL 10034/10064
Manufacturer: VITROLIFE SWEDEN AB
Device Classification Name: media, reproductive
Regulation Number: 884.6180
Classification Product Code: MQL
Date Received: 06/10/2002
Decision Date: 09/06/2002
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: HSA-SOLUTION, MODEL 10034/10064
Manufacturer: VITROLIFE SWEDEN AB
Device Classification Name: media, reproductive
Regulation Number: 884.6180
Classification Product Code: MQL
Date Received: 06/10/2002
Decision Date: 09/06/2002
Regulation Medical Specialty: Obstetrics/Gynecology
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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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