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 |