ELECTROSHIELD
Electrosurgical, Cutting & Coagulation & Accessories
ELECTROSCOPE, INC.
The following data is part of a premarket notification filed by Electroscope, Inc. with the FDA for Electroshield.
Pre-market Notification Details
| Device ID | K912781 |
| 510k Number | K912781 |
| Device Name: | ELECTROSHIELD |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ELECTROSCOPE, INC. 4890 STERLING DR. Boulder, CO 80301 |
| Contact | Roger C.odell |
| Correspondent | Roger C.odell ELECTROSCOPE, INC. 4890 STERLING DR. Boulder, CO 80301 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-06-24 |
| Decision Date | 1991-12-30 |
Trademark Results [ELECTROSHIELD]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ELECTROSHIELD 87306045 5241591 Live/Registered |
ConSeal International Incorporated 2017-01-18 |
 ELECTROSHIELD 76060609 2483848 Dead/Cancelled |
WABASH NATIONAL L.P. 2000-05-31 |
 ELECTROSHIELD 74149562 1732056 Dead/Cancelled |
ENCISION, INC. 1991-03-20 |
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