FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ILLUMIGENE GROUP B STREPTOCOCCUS ,EXTERNAL CONTROL KIT
K Number: K112125
·
Decision Dec 5, 2011
Classifications
1
FEI Numbers
13
Registration Numbers
13
Same Product Code
17
Applicant Total
38
Review Days
133
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Basic Information
- Device Name
- ILLUMIGENE GROUP B STREPTOCOCCUS ,EXTERNAL CONTROL KIT
- K Number
- K112125
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3740
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Meridian Bioscience, Inc.
- Date Received
- July 25, 2011
- Decision Date
- December 5, 2011
- Product Code
- NJR
- Advisory Committee
- Microbiology
- Review Advisory Committee
- MI
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NJR | Nucleic Acid Amplification Assay System, Group B Streptococcus, Direct Specimen Test | FDA class 1 | Microbiology |
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