Antisera, All Groups, N. Meningitidis
FDA product code GTJ · 16 cleared devices
Class 2
Microbiology
- Regulation
- 21 CFR 866.3390
- Review panel
- MI
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 1977-08-25 – 1996-05-30
GTJ
1996-05-30
GTJ
1992-03-23
DIRECTIGEN MENINGITIS COMBO TEST KIT
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GTJ
1991-08-12
SLIDEX MENINGITE-KIT 5
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GTJ
1989-02-07
BACTIGEN(R) N. MENINGITIDIS
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GTJ
1987-03-17
IMMUNOSCAN(TM) DIRECT NEISSERIA MENINGITIDIS KIT
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GTJ
1986-02-04
WELLCOGEN BACTERIAL ANTIGEN KIT
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GTJ
1986-02-04
WELLCOGEN N. MENINGITIDIS B/E. COLI K1 ZL24
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GTJ
1985-10-17
PHADEBACT CSF TEST
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GTJ
1985-06-10
WILLCOGEN MENINGITIDIS KIT ZL25
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GTJ
1985-06-04
MENINGOCOCCUS GROUP B MONOCLONAL ANTIBODY ZM-51
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GTJ
1985-01-25
DIRECTIGEN NEISSENA MENNINGITIDIS GROUP B TEST
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GTJ
1984-07-06
BACTIGEN - N.MENNINIGITIDIS TEST
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GTJ
1984-01-10
WELLCOGEN N. MENINGITIDIS A,C,Y W135
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GTJ
1983-03-09
BACTIGEN-N. MENINGITIDIS
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GTJ
1982-12-30
PHADEBACT CSF TEST 20
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GTJ
1977-08-25
AGGLUTINATING SERUM W135
View details →No matching devices.
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