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FDA 510(k), K150776, Medrobotics Flex System
FDA 510(k), K150776, Medrobotics Flex System
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510(K) Number: K150776
Device Name: Medrobotics Flex System
Manufacturer: MEDROBOTICS CORPORATION
Device Classification Name: nasopharyngoscope (flexible or rigid)
Regulation Number: 874.4760
Classification Product Code: EOB
Date Received: 03/24/2015
Decision Date: 07/17/2015
Regulation Medical Specialty: Ear Nose & Throat
Device Name: Medrobotics Flex System
Manufacturer: MEDROBOTICS CORPORATION
Device Classification Name: nasopharyngoscope (flexible or rigid)
Regulation Number: 874.4760
Classification Product Code: EOB
Date Received: 03/24/2015
Decision Date: 07/17/2015
Regulation Medical Specialty: Ear Nose & Throat
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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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