FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SELECTIVE RAPID UREA
K Number: K883641
·
Decision May 4, 1989
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
137
Review Days
252
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Basic Information
- Device Name
- SELECTIVE RAPID UREA
- K Number
- K883641
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3110
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Applicant
- Remel Co.
- Date Received
- August 25, 1988
- Decision Date
- May 4, 1989
- 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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