FDA 510(k)
FDA class 2
Substantially Equivalent
🇫🇷 France
NG-Test CARBA 5
K Number: K191889
·
Decision Oct 2, 2019
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
2
Applicant Total
2
Review Days
79
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Basic Information
- Device Name
- NG-Test CARBA 5
- K Number
- K191889
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 866.1640
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ng Biotech
- Date Received
- July 15, 2019
- Decision Date
- October 2, 2019
- Product Code
- PTJ
- 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 |
|---|---|---|---|
| PTJ | Phenotypic Test Kit, Non-Susceptible/Elevated Mic Organisms, Cultured Isolates | FDA class 2 | Microbiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (PTJ), ordered by most recent decision date.
NG-Test® CTX-M MULTI
FDA 510(k)
FDA Class 2
·Microbiology
RAPIDEC CARBA NP
FDA 510(k)
FDA Class 2
·Microbiology
Other Clearances by Ng Biotech
| K Number | Device Name | ||
|---|---|---|---|
| K243499 | NG-Test® CTX-M MULTI | Jun 4, 2025 | Substantially Equivalent |