Dialysate Concentrate For Hemodialysis (Liquid Or Powder)
FDA product code KPO · 121 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.5820
- Review panel
- GU
- Implant
- No
- Life sustaining
- Yes
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-04-05 – 2026-08-19
KPO
1986-02-05
KPO
1985-10-31
ULTRACLONE 05-100 GUINEA PIG RBC
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KPO
1985-06-12
HEMODIALYSIS CONCENTRATE ADDITIVES
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KPO
1985-01-09
HEMODIALYSATE SOLUTIONS
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KPO
1984-02-21
LAS-2 ALIGNMENT SYSTEM
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KPO
1983-11-03
HEMO-DIAL
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KPO
1983-01-17
DIALYTE
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KPO
1982-11-17
DIALYSATE ADDITIVES-POWDER/LIQUID
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KPO
1982-05-18
CENTRALYTE BICARBONATE CONCENTRATE
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KPO
1982-01-29
K-AID
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KPO
1982-01-29
DIALYSIS CONCENTRATE
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KPO
1981-12-31
HEMODIALYSATE
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KPO
1981-09-24
LACTIC ACID DIALYSATE ADDITIVE
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KPO
1981-04-23
NATURALYTE BICARBONATE DIALYSATE CONCEN.
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KPO
1981-04-23
CHEM-DIALYTE CONCENTRATES
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KPO
1981-02-19
DIALYSATE CONCENTRATE FOR HEMODIALYSIS
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KPO
1980-07-14
LOW-ACETATE HEMODIALYSIS BATH CONCENTR.
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KPO
1980-04-08
HEMODIALYSIS CONCENTRATE SOLUTION
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KPO
1980-01-04
RENAL SYSTEMS HEMODIALYSIS CONCENTRATE
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KPO
1978-12-07
HEMODIALYSIS CONCENTRATE, SODIU
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KPO
1978-04-05
DRI-LYTE
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