FDA 510(k), K781967, HEMODIALYSIS CONCENTRATE, SODIU
FDA 510(k), K781967, HEMODIALYSIS CONCENTRATE, SODIU
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510(K) Number: K781967
Device Name: HEMODIALYSIS CONCENTRATE, SODIU
Manufacturer: RENAL SYSTEMS, INC.
Device Classification Name: dialysate concentrate for hemodialysis (liquid or powder)
Regulation Number: 876.5820
Classification Product Code: KPO
Date Received: 11/24/1978
Decision Date: 12/07/1978
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: HEMODIALYSIS CONCENTRATE, SODIU
Manufacturer: RENAL SYSTEMS, INC.
Device Classification Name: dialysate concentrate for hemodialysis (liquid or powder)
Regulation Number: 876.5820
Classification Product Code: KPO
Date Received: 11/24/1978
Decision Date: 12/07/1978
Regulation Medical Specialty: Gastroenterology/Urology