Kit, Identification, Neisseria Gonorrhoeae
FDA product code JSX · 16 cleared devices
Class 1
Microbiology
- Regulation
- 21 CFR 866.2660
- Review panel
- MI
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1978-08-31 – 1996-09-18
JSX
1996-09-18
JSX
1992-11-02
NIZYME TEST KIT
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JSX
1991-10-11
VISI-NEISSERIA
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JSX
1988-08-25
XACT NEISSERIA
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JSX
1988-05-18
MODIFIED IDS RAPID NH SYSTEM
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JSX
1987-03-20
NEISSERIA/BRANHAMELLA DIFFERENTIAL TEST
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JSX
1985-09-05
QUAD FERM +
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JSX
1985-07-23
NEISSERIA - KWIK PLUS
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JSX
1985-07-12
GONI-KIT
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JSX
1983-12-27
PHADEBACK G.C. POSITIVE CONTROLS
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JSX
1983-11-14
GONOCHEK-II
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JSX
1983-03-08
NEISSERIA IDENTIFICATION DISCS
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JSX
1981-08-18
IDS RAPIDS NH SYSTEMS
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JSX
1981-06-16
NEISSERIA-KWIK
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JSX
1979-04-23
GONO-CELL
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JSX
1978-08-31
MICROCULT-GC CULTURE TEST
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