The following data is part of a premarket notification filed by Sauter Ag with the FDA for Belimed Steam Sterilizer Mst-v.
| Device ID | K103841 |
| 510k Number | K103841 |
| Device Name: | BELIMED STEAM STERILIZER MST-V |
| Classification | Sterilizer, Steam |
| Applicant | SAUTER AG ZELGSTRASSE 8 Sulgen Tg, CH Ch-8583 |
| Contact | Hans Stadler |
| Product Code | FLE |
| CFR Regulation Number | 880.6880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2010-12-22 |
| Decision Date | 2011-03-15 |
| Summary: | summary |