FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UNI-GOLD H. PYLORI
K Number: K991697
·
Decision Dec 21, 1999
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
5
Review Days
217
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Basic Information
- Device Name
- UNI-GOLD H. PYLORI
- K Number
- K991697
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3110
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Trinity Biotech, Plc
- Date Received
- May 18, 1999
- Decision Date
- December 21, 1999
- Product Code
- LYR
- 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 |
|---|---|---|---|
| LYR | Helicobacter Pylori | FDA class 1 | Microbiology |
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Other Clearances by Trinity Biotech, Plc
| K Number | Device Name | ||
|---|---|---|---|
| K014233 | CAPTIAM SYPHILIS-G ASSAY | Jan 24, 2002 | Substantially Equivalent |
| K011709 | UNI-GOLD STREP A TEST KIT | Nov 8, 2001 | Substantially Equivalent |
| K001525 | CAPTIA SYPHILIS-G ELISA TEST SYSTEM | Nov 29, 2000 | Substantially Equivalent |
| K982373 | UNI-GOLD STREP A TEST KIT | Feb 11, 1999 | Substantially Equivalent |