FDA 510(k), K053052, MEDELA SWING BREAST PUMP
FDA 510(k), K053052, MEDELA SWING BREAST PUMP
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510(K) Number: K053052
Device Name: MEDELA SWING BREAST PUMP
Manufacturer: MEDELA AG
Device Classification Name: Pump, Breast, Powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 10/31/2005
Decision Date: 05/02/2006
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: MEDELA SWING BREAST PUMP
Manufacturer: MEDELA AG
Device Classification Name: Pump, Breast, Powered
Regulation Number: 884.5160
Classification Product Code: HGX
Date Received: 10/31/2005
Decision Date: 05/02/2006
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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