The following data is part of a premarket notification filed by Rita Medical Systems with the FDA for Rita Model 90 Electrosurgical Accessory, Model 90.
| Device ID | K992693 |
| 510k Number | K992693 |
| Device Name: | RITA MODEL 90 ELECTROSURGICAL ACCESSORY, MODEL 90 |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | RITA MEDICAL SYSTEMS 967 NORTH SHORELINE BLVD. Mountain View, CA 94043 |
| Contact | Erin Dignan |
| Correspondent | Erin Dignan RITA MEDICAL SYSTEMS 967 NORTH SHORELINE BLVD. Mountain View, CA 94043 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-12 |
| Decision Date | 1999-09-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| H7877001039091 | K992693 | 000 |
| H7877001013201 | K992693 | 000 |
| H7877001019301 | K992693 | 000 |
| H7877001026151 | K992693 | 000 |
| H7877001039011 | K992693 | 000 |
| H7877001039021 | K992693 | 000 |
| H7877001039031 | K992693 | 000 |
| H7877001039041 | K992693 | 000 |
| H7877001039051 | K992693 | 000 |
| H7877001013171 | K992693 | 000 |