FDA 510(k), K032526, BINDER CO2 INCUBATOR SERIE CB
FDA 510(k), K032526, BINDER CO2 INCUBATOR SERIE CB
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510(K) Number: K032526
Device Name: BINDER CO2 INCUBATOR SERIE CB
Manufacturer: BINDER GMBH
Device Classification Name: accessory, assisted reproduction
Regulation Number: 884.6120
Classification Product Code: MQG
Date Received: 08/15/2003
Decision Date: 08/29/2003
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: BINDER CO2 INCUBATOR SERIE CB
Manufacturer: BINDER GMBH
Device Classification Name: accessory, assisted reproduction
Regulation Number: 884.6120
Classification Product Code: MQG
Date Received: 08/15/2003
Decision Date: 08/29/2003
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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