The following data is part of a premarket notification filed by Lexion Medical, Llc. with the FDA for Vessel Guardian.
| Device ID | K102136 |
| 510k Number | K102136 |
| Device Name: | VESSEL GUARDIAN |
| Classification | Insufflator, Laparoscopic |
| 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 | HIF |
| CFR Regulation Number | 884.1730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-07-29 |
| Decision Date | 2010-09-27 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00852588007076 | K102136 | 000 |