The following data is part of a premarket notification filed by Soring Gmbh Medizintechnik with the FDA for Soring Gmbh Sonoca 180/190.
| Device ID | K012753 |
| 510k Number | K012753 |
| Device Name: | SORING GMBH SONOCA 180/190 |
| Classification | Instrument, Ultrasonic Surgical |
| Applicant | SORING GMBH MEDIZINTECHNIK 1100 LAKEVIEW BLVD. Denton, TX 76208 |
| Contact | Carl Alletto |
| Correspondent | Carl Alletto SORING GMBH MEDIZINTECHNIK 1100 LAKEVIEW BLVD. Denton, TX 76208 |
| Product Code | LFL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-08-16 |
| Decision Date | 2001-11-13 |
| Summary: | summary |