FDA 510(k), K170934, C3 Wave System
FDA 510(k), K170934, C3 Wave System
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$149.00 USD
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510(K) Number: K170934
Device Name: C3 Wave System
Manufacturer: Courtney Nix
Device Classification Name: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation Number: LJS
Classification Product Code: 03/30/2017
Date Received: 12/06/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: C3 Wave System
Manufacturer: Courtney Nix
Device Classification Name: Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Regulation Number: LJS
Classification Product Code: 03/30/2017
Date Received: 12/06/2017
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital