The following data is part of a premarket notification filed by Lipose Corp. with the FDA for Lipose Disposable Cannula.
| Device ID | K093067 |
| 510k Number | K093067 |
| Device Name: | LIPOSE DISPOSABLE CANNULA |
| Classification | System, Suction, Lipoplasty |
| Applicant | LIPOSE CORP. 1205 DE LA VINA STREET Santa Barbara, CA 93101 |
| Contact | Christine Emanuel |
| Correspondent | Christine Emanuel LIPOSE CORP. 1205 DE LA VINA STREET Santa Barbara, CA 93101 |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-30 |
| Decision Date | 2009-12-29 |
| Summary: | summary |