The following data is part of a premarket notification filed by World Of Medicine Lemke Gmbh with the FDA for Endoscopic Light Source Xl202/l3.
Device ID | K020889 |
510k Number | K020889 |
Device Name: | ENDOSCOPIC LIGHT SOURCE XL202/L3 |
Classification | Light Source, Endoscope, Xenon Arc |
Applicant | WORLD OF MEDICINE LEMKE GMBH 91 TROWBRIDGE ST. Cambridge, MA 02138 |
Contact | Susanne Raab |
Correspondent | Susanne Raab WORLD OF MEDICINE LEMKE GMBH 91 TROWBRIDGE ST. Cambridge, MA 02138 |
Product Code | GCT |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-03-19 |
Decision Date | 2002-06-05 |
Summary: | summary |