Dialyzer, High Permeability With Or Without Sealed Dialysate System
FDA product code KDI · 332 cleared devices
Class 2
Gastroenterology, Urology
- Regulation
- 21 CFR 876.5860
- Review panel
- GU
- Implant
- No
- Life sustaining
- Yes
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-12-20 – 2026-07-24
KDI
1984-07-06
KDI
1984-04-20
CENTRY 2000 DIALYSIS CONTROL UNIT
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KDI
1984-03-23
BLOOD CONCENTRATOR 140
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KDI
1984-03-23
AMICON DIAFILTER 40. HEMOFILTER
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KDI
1984-02-04
BIOSPAL (R) 1800S
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KDI
1984-02-04
HEMOFILTRATION SYSTEM
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KDI
1984-01-03
ULTRAFILTRATION CONTROLLER
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KDI
1983-09-20
BIOSPAL 1200S
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KDI
1983-09-20
BIOSPAL 3000 S
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KDI
1983-04-28
MONITRAL
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KDI
1983-04-28
HEMO-PROCESSING SYSTEM
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KDI
1983-04-27
ULTRAFILTRATION MONITOR UFM-10-2
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KDI
1983-03-29
H1207
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KDI
1983-03-29
H1210
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KDI
1983-03-02
FH 101, FH 202 & FH 303 FIBER HEMOFILTER
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KDI
1983-01-17
ARTERIOVENOUS BLOOD TUBING SET FOR
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KDI
1983-01-07
COBE HEMOCONCENTRATOR 1.3
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KDI
1982-12-22
H 12 07
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KDI
1982-12-16
AMICON DIAFILTERS 20 & 30 HEMOFILTERS
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KDI
1982-03-31
HEMOFILTERS
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KDI
1982-03-25
CONTINUOUS BLOOD PROCESSOR CBP-6000 &
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KDI
1981-10-19
MODEL H12-10
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KDI
1981-09-21
C-DAK DUO-FLUX ARTIFICIAL KIDNEY
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KDI
1981-08-31
GAMBRO LUNDIA PLATE HIGH FLUX DIALYZER
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KDI
1980-08-27
GAMBRO LUNDIA MAJOR HIGH FLUX HEMODIALYZ
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KDI
1980-08-27
GAMBRO LUNDIA PLATE HIGH FLUX HEMODIAL-
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KDI
1980-08-13
C-DAK DUO-FLUX ARTIFICIAL KIDNEY
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KDI
1980-08-07
MODEL H 607-.67M2 30 MICRON RP AN69 MEM
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KDI
1980-07-28
MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TEST
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KDI
1979-09-04
RP-610 PARALLEL PLATE DIALYZER
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KDI
1978-12-20
HEMODIALYZER, MODEL RP610, RP AN 69
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KDI
1978-12-20
CORTRAL I
View details →No matching devices.
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