System, Test, Systemic Lupus Erythematosus
FDA product code DHC · 16 cleared devices
Class 2
Immunology
- Regulation
- 21 CFR 866.5820
- Review panel
- IM
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1979-03-12 – 2001-04-09
DHC
2001-04-09
DHC
2001-03-30
REAADS IGM ANTI-PROTHROMBIN SEMI-QUANTITATIVE TEST KIT
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DHC
1993-03-10
ELIAS DSDNA ABS
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DHC
1993-03-10
HUMAN A-DS DNA EIA KIT FOR DIAGNOSTIC USE
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DHC
1991-12-09
IMMUNOWELL DSDNA ANTIBODY TEST
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DHC
1989-01-24
ACCESS R-CLONE ANA PROFILE ASSAY
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DHC
1987-08-12
IMMUNO/SLE
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DHC
1982-05-28
SERO/TEX LE TEST
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DHC
1981-04-29
ANTI NDNA IMMUNOFLOURESCENT TEST SYS
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DHC
1981-02-09
SLE ANTI-N-DNA LATEX TEST
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DHC
1980-05-08
CORDIA NP
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DHC
1980-05-08
CORDIA N
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DHC
1980-04-02
ANA LATEX SLIDE TEST
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DHC
1979-03-15
SYSTEMIC LUPUS
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DHC
1979-03-15
IIF-A-N-DNA TEST KIT
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DHC
1979-03-12
LUPO-TEC
View details →No matching devices.
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