FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MERETEK UBT_LITE BREATH TEST FOR H. PYLORI
K Number: K000316
·
Decision Feb 24, 2000
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
16
Applicant Total
1
Review Days
23
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Basic Information
- Device Name
- MERETEK UBT_LITE BREATH TEST FOR H. PYLORI
- K Number
- K000316
- Device Class
- FDA class 1
- Clearance Type
- Special
- Regulation Number
- 866.3110
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Meretek
- Date Received
- February 1, 2000
- Decision Date
- February 24, 2000
- Product Code
- MSQ
- 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 |
|---|---|---|---|
| MSQ | Test, Urea (Breath Or Blood) | FDA class 1 | Microbiology |
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