The following data is part of a premarket notification filed by Lmt Lammers Medical Technology Gmbh with the FDA for Lmt Nomag Ic 3.0.
| Device ID | K062052 |
| 510k Number | K062052 |
| Device Name: | LMT NOMAG IC 3.0 |
| Classification | Incubator, Neonatal Transport |
| Applicant | LMT LAMMERS MEDICAL TECHNOLOGY GMBH OSTERWEIDE 8 Luebeck, DE 23568 |
| Contact | Thomas M Bohnen |
| Correspondent | Jeffrey D Rongero UNDERWRITERS LABORATORIES, INC. 12 LABORATORY DR. Research Triangle, NC 27709 |
| Product Code | FPL |
| CFR Regulation Number | 880.5410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2006-07-20 |
| Decision Date | 2006-07-31 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04260486610032 | K062052 | 000 |
| 04260486610575 | K062052 | 000 |