The following data is part of a premarket notification filed by Shina Systems Ltd. with the FDA for 3di.
| Device ID | K113442 |
| 510k Number | K113442 |
| Device Name: | 3DI |
| Classification | System, Image Processing, Radiological |
| Applicant | SHINA SYSTEMS LTD. 6 SIRENI Haifa, IL 32972 |
| Contact | Dan Laor |
| Correspondent | Dan Laor SHINA SYSTEMS LTD. 6 SIRENI Haifa, IL 32972 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-21 |
| Decision Date | 2012-02-16 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07290018235003 | K113442 | 000 |