The following data is part of a premarket notification filed by Stentor, Inc. with the FDA for Stentor, Pageview.
| Device ID | K992698 |
| 510k Number | K992698 |
| Device Name: | STENTOR, PAGEVIEW |
| Classification | System, Digital Image Communications, Radiological |
| Applicant | STENTOR, INC. 16303 PANORAMIC WAY San Leandro, CA 94578 |
| Contact | Gary J Allsebrook |
| Correspondent | Gary J Allsebrook STENTOR, INC. 16303 PANORAMIC WAY San Leandro, CA 94578 |
| Product Code | LMD |
| CFR Regulation Number | 892.2020 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-11 |
| Decision Date | 1999-10-25 |
| Summary: | summary |