The following data is part of a premarket notification filed by Soring Gmbh Medizintechnik with the FDA for Soring Gmbh, Arco 3000, Arco 2000, Arco 1000, Mbc 601, Mbc 600.
| Device ID | K993265 |
| 510k Number | K993265 |
| Device Name: | SORING GMBH, ARCO 3000, ARCO 2000, ARCO 1000, MBC 601, MBC 600 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | SORING GMBH MEDIZINTECHNIK 3200 DOGWOOD COURT Cincinnati, OH 45140 |
| Contact | Carl Alletto |
| Correspondent | Carl Alletto SORING GMBH MEDIZINTECHNIK 3200 DOGWOOD COURT Cincinnati, OH 45140 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-09-29 |
| Decision Date | 1999-10-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04250321532575 | K993265 | 000 |
| 04250321513666 | K993265 | 000 |
| 04250321513673 | K993265 | 000 |
| 04250321513680 | K993265 | 000 |
| 04250321513697 | K993265 | 000 |
| 04250321513710 | K993265 | 000 |
| 04250321513734 | K993265 | 000 |
| 04250321518722 | K993265 | 000 |
| 04250321527403 | K993265 | 000 |
| 04250321528325 | K993265 | 000 |
| 04250321532315 | K993265 | 000 |
| 04250321508167 | K993265 | 000 |