The following data is part of a premarket notification filed by Stellartech Research Corp. with the FDA for Modification To: Stellartech Coagulation System (models 1100c-115 & 1100c-230).
| Device ID | K032721 |
| 510k Number | K032721 |
| Device Name: | MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230) |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | STELLARTECH RESEARCH CORP. 1346 BORDEAUX DR. Sunnyvale, CA 94089 |
| Contact | Gary A Seeger |
| Correspondent | Gary A Seeger STELLARTECH RESEARCH CORP. 1346 BORDEAUX DR. Sunnyvale, CA 94089 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-09-03 |
| Decision Date | 2003-10-06 |
| Summary: | summary |