FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
PYLORIPROBE
K Number: K981396
·
Decision Jul 30, 1998
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
90
Applicant Total
2
Review Days
104
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Basic Information
- Device Name
- PYLORIPROBE
- K Number
- K981396
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 866.3110
- Medical Specialty
- Microbiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Amdl, Inc.
- Date Received
- April 17, 1998
- Decision Date
- July 30, 1998
- 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 Amdl, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K072901 | AMDL-ELISA DR-70 (FDP) IMMUNOASSAY, MODEL DR2101 | Jul 1, 2008 | Substantially Equivalent |