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FDA 510(k), K182732, JTL-250-01
FDA 510(k), K182732, JTL-250-01
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$149.00 USD
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510(K) Number: K182732
Device Name: JTL-250-01
Manufacturer: Jointechlabs, Inc.
Device Classification Name: System, Suction, Lipoplasty
Regulation Number: 878.5040
Classification Product Code: MUU
Date Received: 09/28/2018
Decision Date: 11/18/2019
Regulation Medical Specialty: General & Plastic Surgery
Device Name: JTL-250-01
Manufacturer: Jointechlabs, Inc.
Device Classification Name: System, Suction, Lipoplasty
Regulation Number: 878.5040
Classification Product Code: MUU
Date Received: 09/28/2018
Decision Date: 11/18/2019
Regulation Medical Specialty: General & Plastic Surgery
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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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