The following data is part of a premarket notification filed by Lexion Medical, Llc. with the FDA for Insuflow Co2ionshield.
| Device ID | K090879 |
| 510k Number | K090879 |
| Device Name: | INSUFLOW CO2IONSHIELD |
| Classification | Insufflator, Automatic Carbon-dioxide For Endoscope |
| Applicant | LEXION MEDICAL, LLC. 5000 TOWNSHIP PKWY St. Paul, MN 55110 |
| Contact | Bernard Horwath |
| Correspondent | Bernard Horwath LEXION MEDICAL, LLC. 5000 TOWNSHIP PKWY St. Paul, MN 55110 |
| Product Code | FCX |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-03-31 |
| Decision Date | 2009-07-23 |
| Summary: | summary |