The following data is part of a premarket notification filed by Millennium Medical Technologies, Inc. with the FDA for Lipo Cannula.
| Device ID | K081039 |
| 510k Number | K081039 |
| Device Name: | LIPO CANNULA |
| Classification | System, Suction, Lipoplasty |
| Applicant | MILLENNIUM MEDICAL TECHNOLOGIES, INC. 7055 DIVOT DR. Laverne, CA 91750 |
| Contact | Gregory M Miles |
| Correspondent | Gregory M Miles MILLENNIUM MEDICAL TECHNOLOGIES, INC. 7055 DIVOT DR. Laverne, CA 91750 |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-04-11 |
| Decision Date | 2008-07-10 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00850421007139 | K081039 | 000 |
| 00850421007030 | K081039 | 000 |
| 00850000712393 | K081039 | 000 |
| 00850000712386 | K081039 | 000 |
| 00850000712300 | K081039 | 000 |
| 00850000712287 | K081039 | 000 |