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FDA 510(k), K161038, PK Morcellator
FDA 510(k), K161038, PK Morcellator
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510(K) Number: K161038
Device Name: PK Morcellator
Manufacturer: GRAHAM A.L. BAILLIE
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: KXA
Date Received: 04/13/2016
Decision Date: 10/07/2016
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: PK Morcellator
Manufacturer: GRAHAM A.L. BAILLIE
Device Classification Name: Electrosurgical, Cutting & Coagulation & Accessories
Regulation Number: GEI
Classification Product Code: KXA
Date Received: 04/13/2016
Decision Date: 10/07/2016
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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