The following data is part of a premarket notification filed by The Gid Group, Inc. with the FDA for Gid 700.
| Device ID | K120902 |
| 510k Number | K120902 |
| Device Name: | GID 700 |
| Classification | System, Suction, Lipoplasty |
| Applicant | THE GID GROUP, INC. 4655 KIRKWOOD COURT Boulder, CO 80301 |
| Contact | Lewis Ward |
| Correspondent | Lewis Ward THE GID GROUP, INC. 4655 KIRKWOOD COURT Boulder, CO 80301 |
| Product Code | MUU |
| CFR Regulation Number | 878.5040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-26 |
| Decision Date | 2012-08-15 |
| Summary: | summary |