NICO Myriad
Electrosurgical, Cutting & Coagulation & Accessories
NICO Corporation
The following data is part of a premarket notification filed by Nico Corporation with the FDA for Nico Myriad.
Pre-market Notification Details
| Device ID | K182340 |
| 510k Number | K182340 |
| Device Name: | NICO Myriad |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | NICO Corporation 250 East 96th Street, Suite 125 Indianapolis, IN 46240 |
| Contact | Sean Spence |
| Correspondent | Sean Spence NICO Corporation 250 East 96th Street, Suite 125 Indianapolis, IN 46240 |
| Product Code | GEI |
| Subsequent Product Code | ERL |
| Subsequent Product Code | HBC |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-28 |
| Decision Date | 2018-09-20 |
| Summary: | summary |
Trademark Results [NICO Myriad]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NICO MYRIAD 88356482 5879212 Live/Registered |
Nico Corporation 2019-03-26 |
 NICO MYRIAD 77608038 3761740 Live/Registered |
Nico Corporation 2008-11-05 |
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