FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
LMT NOMAG IC 3.0
K Number: K062052
·
Decision Jul 31, 2006
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
24
Applicant Total
2
Review Days
11
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Basic Information
- Device Name
- LMT NOMAG IC 3.0
- K Number
- K062052
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5410
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Lmt Lammers Medical Technology GmbH
- Date Received
- July 20, 2006
- Decision Date
- July 31, 2006
- Product Code
- FPL
- 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 |
|---|---|---|---|
| FPL | Incubator, Neonatal Transport | FDA class 2 | General Hospital |
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Other Clearances by Lmt Lammers Medical Technology GmbH
| K Number | Device Name | ||
|---|---|---|---|
| K033565 | LMT NOMAG IC 1,5 | Nov 21, 2003 | Substantially Equivalent |