The following data is part of a premarket notification filed by Sciton, Inc. with the FDA for Joule 810/940/980 Multi-platform System.
| Device ID | K122567 |
| 510k Number | K122567 |
| Device Name: | JOULE 810/940/980 MULTI-PLATFORM SYSTEM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | SCITON, INC. 925 COMMERCIAL STREET Palo Alto, CA 94303 |
| Contact | Jay M Patel |
| Correspondent | Jay M Patel SCITON, INC. 925 COMMERCIAL STREET Palo Alto, CA 94303 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-08-23 |
| Decision Date | 2013-06-19 |
| Summary: | summary |