The following data is part of a premarket notification filed by Mim Software Inc. with the FDA for Mim-thin Client (mobile).
| Device ID | K151913 |
| 510k Number | K151913 |
| Device Name: | MIM-Thin Client (mobile) |
| Classification | System, Image Processing, Radiological |
| Applicant | MIM Software Inc. 25800 Science Park Drive SUITE 180 Cleveland, OH 44122 |
| Contact | Lynn Hanigan |
| Correspondent | Lynn Hanigan MIM Software Inc. 25800 Science Park Drive SUITE 180 Cleveland, OH 44122 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-13 |
| Decision Date | 2016-04-25 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00865936000230 | K151913 | 000 |