The following data is part of a premarket notification filed by Earlysense Ltd. with the FDA for Everon 1.0.
| Device ID | K092062 |
| 510k Number | K092062 |
| Device Name: | EVERON 1.0 |
| Classification | Monitor, Breathing Frequency |
| Applicant | EARLYSENSE LTD. TZVI 12 Ramat-gan, IL 52504 |
| Contact | Dalia Argaman |
| Correspondent | Dalia Argaman EARLYSENSE LTD. TZVI 12 Ramat-gan, IL 52504 |
| Product Code | BZQ |
| CFR Regulation Number | 868.2375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-07-08 |
| Decision Date | 2010-05-24 |
| Summary: | summary |