The following data is part of a premarket notification filed by Soring Gmbh Medizintechnik with the FDA for Soring Mbc200/bcc140.
| Device ID | K093511 |
| 510k Number | K093511 |
| Device Name: | SORING MBC200/BCC140 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | SORING GMBH MEDIZINTECHNIK JUSTUS-V. LIEBIG 2 Quickborn, DE 25451 |
| Contact | Jan Schueller-iwersen |
| Correspondent | Jan Schueller-iwersen SORING GMBH MEDIZINTECHNIK JUSTUS-V. LIEBIG 2 Quickborn, DE 25451 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-11-13 |
| Decision Date | 2010-04-16 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04250321532483 | K093511 | 000 |
| 04250321532346 | K093511 | 000 |