The following data is part of a premarket notification filed by Immersive Touch with the FDA for Immersivetouch3 And Microvistouch.
| Device ID | K140860 |
| 510k Number | K140860 |
| Device Name: | ImmersiveTouch3 And MicrovisTouch |
| Classification | System, Image Processing, Radiological |
| Applicant | IMMERSIVE TOUCH 708 KRISTIN COURT Westmont, IL 60559 |
| Contact | Prashant Banerjee |
| Correspondent | Prashant Banerjee IMMERSIVE TOUCH 708 KRISTIN COURT Westmont, IL 60559 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-04-03 |
| Decision Date | 2014-12-16 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B940IVZBKIT0 | K140860 | 000 |
| B940IMMERSIVEVIEW0 | K140860 | 000 |