Kit, Screening, Staphylococcus Aureus
FDA product code JWX · 20 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
- 1981-05-05 – 2009-12-16
JWX
2009-12-16
JWX
1997-09-08
STAPHYTECT PLUS/DRYSPOT STAPHYTECT PLUS
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JWX
1997-02-07
REMEL STAPH LATEX KIT
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JWX
1995-06-01
STAPHAUREX PLUS(TM)
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JWX
1993-08-10
STAPH-A-LEX(TM) SYSTEM
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JWX
1992-09-28
SLIDEX STAPH-KIT
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JWX
1991-03-29
VISI-STAPH
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JWX
1990-06-18
AXIOM TOTAL KNEE SYSTEM, TIBIAL COMPONENT
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JWX
1987-10-28
STAPHSLIDE
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JWX
1986-03-04
NEG COMBO BREAKPOINT PANEL POS COMBO
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JWX
1986-03-03
V-TREND KIT STAPH LATEX TEST
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JWX
1985-08-19
RAPI - STAPH
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JWX
1984-10-01
BACTO STAPHYLOCOCCUS LATEX TEST
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JWX
1983-06-08
LA-STAPH IDENTIFICATION SYSTEM
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JWX
1983-04-08
VERI-STAPH
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JWX
1982-09-14
LSM AGAR
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JWX
1982-08-24
IDS STAPHYLOCHROME TEST
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JWX
1982-07-30
BBL STAPHYSLIDE TEST
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JWX
1982-02-04
STAPH TRAC
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JWX
1981-05-05
SERO-STAT STAPHYLOCOCCUS TEST
View details →No matching devices.
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