FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇷 Greece
MICROPUMP MP-101
K Number: K051252
·
Decision May 27, 2005
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
1
Review Days
11
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Basic Information
- Device Name
- MICROPUMP MP-101
- K Number
- K051252
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Micrel Medical Devices S.A.
- Date Received
- May 16, 2005
- Decision Date
- May 27, 2005
- Product Code
- FRN
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- Third Party
- Y
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| FRN | Pump, Infusion | FDA class 2 | General Hospital |
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