The following data is part of a premarket notification filed by Asclepion Laser Technologies Gmbh with the FDA for Multipulse Hoplus.
| Device ID | K131987 |
| 510k Number | K131987 |
| Device Name: | MULTIPULSE HOPLUS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | ASCLEPION LASER TECHNOLOGIES GMBH BRUESSELER STR. 10 Jena, Thuringia, DE 07747 |
| Contact | Antje Katzer |
| Correspondent | Antje Katzer ASCLEPION LASER TECHNOLOGIES GMBH BRUESSELER STR. 10 Jena, Thuringia, DE 07747 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-06-28 |
| Decision Date | 2014-10-15 |
| Summary: | summary |