Reagents, Antibody, Legionella, Direct & Indirect Fluorescent
FDA product code LHL · 18 cleared devices
Class 2
Microbiology
- Regulation
- 21 CFR 866.3300
- Review panel
- MI
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1981-09-08 – 1999-01-11
LHL
1999-01-11
LHL
1997-06-18
LEGIONELLA ELISA TEST SYSTEM
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LHL
1997-03-03
LEGIONELLA IGG/IGM ELISA TEST SYSTEM
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LHL
1992-07-28
LEGIONELLA REAGENS FOR DIRECT FLUORESCENT ANTIBODY
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LHL
1987-09-02
DU PONT LEGIONELLA URINARY ANTIGEN - RIA KIT
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LHL
1987-04-20
LEGIONELLA PNEUMOPHILA SER. 1 ANTIGEN LATEX TEST
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LHL
1985-11-12
POLYVALENT FLUORESCENT ANTIBODY REAGENTS FOR LEGIO
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LHL
1985-08-22
LEGIONELLA IMMUNOFLUORESCENT ANTIBODY TEST KIT
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LHL
1984-08-02
GENETIC SYS LEGIONELLA IMMUNOFLURORES
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LHL
1983-10-14
LEGIONELLA INDIRECT FLUORESCENT ANTIBOD
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LHL
1983-08-08
LEGIONELLA IFA KIT I
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LHL
1983-06-22
INDIRECT FLUORESCENT ANTIBODY REAGENTS
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LHL
1983-06-08
LEGIONELLA DFA KIT I
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LHL
1983-02-16
DIRECT FA CONJUGATE FOR LEGIONELLA SPP
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LHL
1982-09-21
LEGIONELLA PNEUMOPHILA
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LHL
1981-12-18
DIRECT FA CONJUGATE FOR LEGIONELLA SP
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LHL
1981-09-08
LEGIONELLA INDIRECT FLUOR. ANTIBODY
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LHL
1981-09-08
LEGIONELLA DIRECT FLUORESCENT ANTIBODY
View details →No matching devices.
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