Assay, Erythropoietin
FDA product code GGT · 20 cleared devices
Class 2
Hematology
- Regulation
- 21 CFR 864.7250
- Review panel
- HE
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1984-03-23 – 2024-04-22
GGT
2024-04-22
GGT
2019-08-02
ADVIA Centaur Erythropoietin (EPO) assay
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GGT
2006-10-06
ACCESS EPO ASSAY
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GGT
2000-06-07
SANGUI BIOTECH, INC. EPO (ERYTHROPOIETIN) ELISA KIT
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GGT
1999-07-12
IMMULITE EPO, MODEL #'S LKEPZ & LKEP1
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GGT
1999-03-23
ADVANTAGE CHEMILUMINESCENCE ERYTHROPOIETIN IMMUNOASSAY
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GGT
1996-05-29
ERYTHROPOIETIN IMMUNOASSAY KIT
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GGT
1996-02-05
PREDICTA ERYTHROPOIETIN KIT (MODIFICATION)
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GGT
1994-07-19
QUANTIKINE IVD ERYTHROPOIETIN ENZYME LINKED IMMUNOSORBENT ASSAY (ELISA)
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GGT
1994-04-21
QUANTIKINE(TM) ERYTHROPOIETIN HUMAN SERUM CONTROLS
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GGT
1994-03-11
ERYTHROPOIETIN IMMUNOASSAY KIT
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GGT
1993-07-20
QUANTIKINE(TM) ERYTHROPOIETIN/ENZ LINK IMMUN ASSAY
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GGT
1993-06-25
PREDICTA ERYTHROPOIETIN KIT
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GGT
1991-11-29
EPO-RIA
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GGT
1990-10-26
DSL ERYTHROPOIETIN (DSL # 1100)
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GGT
1990-08-22
EPO-TRAC(TM) 125I RADIOIMMUNOASSAY (RIA)
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GGT
1989-11-21
EPO-TRAC BY RADIOIMMUNOASSAY (RIA)
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GGT
1989-10-10
CLINIGEN ERYTHROPOIETIN HUMAN SERUM CONTROLS 1,2,3
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GGT
1988-12-20
ERYTHROPOIETIN ENZYME IMMUNOASSAY
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GGT
1984-03-23
ERYTHROPOIETIN EIA
View details →No matching devices.
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