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FDA 510(k), K132744, ACESSA GUIDANCE SYSTEM
FDA 510(k), K132744, ACESSA GUIDANCE SYSTEM
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510(K) Number: K132744
Device Name: ACESSA GUIDANCE SYSTEM
Manufacturer: CLARISA TATE
Device Classification Name: Coagulator, Laparoscopic, Unipolar (And Accessories)
Regulation Number: HFG
Classification Product Code: 09/03/2013
Date Received: 05/27/2014
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: ACESSA GUIDANCE SYSTEM
Manufacturer: CLARISA TATE
Device Classification Name: Coagulator, Laparoscopic, Unipolar (And Accessories)
Regulation Number: HFG
Classification Product Code: 09/03/2013
Date Received: 05/27/2014
Decision Date: Substantially Equivalent (SESE)
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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