LMT NOMAG IC 3.0
FDA 510(k) clearance K062052 · decided 2006-07-31
Clearance details
- K-number
- K062052
- Device name
- LMT NOMAG IC 3.0
- Applicant
- Lmt Lammers Medical Technology GmbH
- Decision
- Substantially Equivalent
- Date received
- 2006-07-20
- Decision date
- 2006-07-31
- Days to decision
- 11 days
- Clearance type
- Traditional
- Product code
- FPL
- Device class
- 2
- Regulation number
- 880.5410
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- Luebeck, DE
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.