Test, Sickle Cell
FDA product code GHM · 18 cleared devices
Class 2
Hematology
- Regulation
- 21 CFR 864.7825
- Review panel
- HE
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1979-11-05 – 2002-12-30
GHM
2002-12-30
GHM
2001-11-06
SICKLE-CHEX
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GHM
1996-07-01
SAS SICKLE CELL TEST
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GHM
1991-10-09
HEMOCARD HEMOGLOBIN S
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GHM
1991-04-15
HEMOCARD-AS
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GHM
1987-07-31
THROMBOSCREEN JOSHUA HEMOGLOBIN S SCREENING KIT
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GHM
1986-04-11
SICKLE CELL REAGENT SET
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GHM
1986-02-24
SICKLE CELL REAGENT SET
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GHM
1985-10-31
THROMBO SCREEN SICKLE CELL ASSAY SET
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GHM
1984-09-09
SICKLING HEMOGLOBIN CONTROLS, NORMAL
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GHM
1984-08-09
SICKLE-HEME A/S HETEROZYGOUS CONTROL
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GHM
1984-07-20
SICKLE CELL REAGENT SET
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GHM
1984-04-13
SICKLE-STAT HEMOGLOBIN S SCREEN KIT
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GHM
1984-04-04
SICKLE HB ASSAY
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GHM
1983-07-28
SICKLE-HEME A/S CONTROLS & A/A CONTROL
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GHM
1982-04-14
SICKLE-CHECK
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GHM
1981-08-12
SICKLE CELL REAGENT SET
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GHM
1979-11-05
MONOJECT SICKLE CELL KIT
View details →No matching devices.
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