System, Dialysate Delivery, Sorbent Regenerated
FDA product code FKT · 19 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.5600
- Review panel
- GU
- Implant
- No
- Life sustaining
- Yes
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1980-01-16 – 2013-02-15
FKT
2013-02-15
FKT
2010-08-13
2008 HEMODIALYSIS SORBENT SYSTEM
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FKT
2007-05-25
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL# 1500
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FKT
2006-05-24
ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100
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FKT
2005-06-03
ALLIENT SORBENT HEMODIALYSIS SYSTEM, MODEL 1000
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FKT
2003-09-17
SORB+HISORB+CARTRIDGE
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FKT
1996-08-28
REDY 2000 SYSTEM (THERAPEUTIC PLASMA EXCHANGE OPTION AND MONITORING LINE Y-CONNECTOR)
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FKT
1988-10-25
REDY 2000
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FKT
1988-04-08
MODIFIED BIOLOGIC 1000 HEMODIAL. & HD-1000 DIS CAR
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FKT
1987-02-25
MODIFIED BIO. HEMODIALYSIS & HD-1000 DISP. CART.
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FKT
1986-12-11
BIOLOGIC 1000 HEMODIALYSIS MACH/HD-1000 DISP CARTR
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FKT
1985-04-12
PACKETS FOR PREP. OF DIALYSATES & INFUSATES -
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FKT
1984-09-12
HEMOPERFUSION PROCEDURE W/REDY 2000
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FKT
1982-03-23
SORB II
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FKT
1981-12-08
D-3260 SORBENT CARTRIDGE
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FKT
1981-07-31
D-3160 SORBENT CARTRIDGE
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FKT
1980-07-21
SORB 10 DIALYSATE INFUSATE C1 INFUSATE
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FKT
1980-07-21
K1 POTASSIUM ACETATE ADDITIVE
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FKT
1980-01-16
SORB SYSTEM URS
View details →No matching devices.
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