The following data is part of a premarket notification filed by Fujifilm Medical Systems U.s.a., Inc. with the FDA for Synapse 3d Nodule Analysis.
| Device ID | K120679 |
| 510k Number | K120679 |
| Device Name: | SYNAPSE 3D NODULE ANALYSIS |
| Classification | System, Image Processing, Radiological |
| Applicant | FUJIFILM MEDICAL SYSTEMS U.S.A., INC. 419 WEST AVE. Stamford, CT 06902 -6300 |
| Contact | Jyh-shyan Lin |
| Correspondent | Jyh-shyan Lin FUJIFILM MEDICAL SYSTEMS U.S.A., INC. 419 WEST AVE. Stamford, CT 06902 -6300 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-06 |
| Decision Date | 2012-06-01 |
| Summary: | summary |