Enzyme Immunoassay, Ethosuximide
FDA product code DLF · 9 cleared devices
Class 2
Clinical Toxicology
- Regulation
- 21 CFR 862.3380
- Review panel
- TX
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1978-04-12 – 1988-06-01
DLF
1988-06-01
DLF
1985-02-06
TDX ETHOSUXIMIDE
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DLF
1984-12-11
EMIT QST ETHOSUXIMIDE ASSAY
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DLF
1983-09-29
MODIFICA- OF EMIT AED ETHOSUXIMIDE ASSAY
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DLF
1983-01-14
AMES TDA ETHOSUXIMIDE TEST
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DLF
1983-01-07
ADVANCE EMIT-AED ETHOSUXIMIDE
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DLF
1979-12-31
ACA ETHOSURIMIDE TEST PACK
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DLF
1978-04-12
ANALYZER-SUPPLEMENT, KINETIC, LKB 2086
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DLF
1978-04-12
ANALYZER, FAST, CENTRIFUGAL, GEMSAEC
View details →No matching devices.
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