FDA 510(k), K952566, OSCILFLATOR
FDA 510(k), K952566, OSCILFLATOR
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510(K) Number: K952566
Device Name: OSCILFLATOR
Manufacturer: SURGICAL TECHNOLOGIES, INC.
Device Classification Name: syringe, balloon inflation
Regulation Number: 870.1650
Classification Product Code: MAV
Date Received: 06/02/1995
Decision Date: 08/31/1995
Regulation Medical Specialty: Cardiovascular
Device Name: OSCILFLATOR
Manufacturer: SURGICAL TECHNOLOGIES, INC.
Device Classification Name: syringe, balloon inflation
Regulation Number: 870.1650
Classification Product Code: MAV
Date Received: 06/02/1995
Decision Date: 08/31/1995
Regulation Medical Specialty: Cardiovascular
- 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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