The following data is part of a premarket notification filed by Sutter Medizintechnik Gmbh with the FDA for Sutter Electrosurgical Cables.
| Device ID | K073450 |
| 510k Number | K073450 |
| Device Name: | SUTTER ELECTROSURGICAL CABLES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | SUTTER MEDIZINTECHNIK GMBH 353 LOMA LARGA ROAD Corrales, NM 87048 |
| Contact | Thomas A Boone |
| Correspondent | Thomas A Boone SUTTER MEDIZINTECHNIK GMBH 353 LOMA LARGA ROAD Corrales, NM 87048 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-12-10 |
| Decision Date | 2008-03-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884524001869 | K073450 | 000 |
| 10381780099482 | K073450 | 000 |
| 10381780099499 | K073450 | 000 |
| 10381780099505 | K073450 | 000 |
| 10381780099512 | K073450 | 000 |
| 10381780099529 | K073450 | 000 |
| 10381780099635 | K073450 | 000 |
| 10381780099642 | K073450 | 000 |
| 10381780099659 | K073450 | 000 |
| 10381780099666 | K073450 | 000 |
| 10884524001852 | K073450 | 000 |
| 10884524001876 | K073450 | 000 |
| 10381780490241 | K073450 | 000 |
| 10381780490340 | K073450 | 000 |
| 10381780099475 | K073450 | 000 |