ACCUCON
Lens, Contact (other Material) - Daily
INNOVISION, INC.
The following data is part of a premarket notification filed by Innovision, Inc. with the FDA for Accucon.
Pre-market Notification Details
| Device ID | K944223 |
| 510k Number | K944223 |
| Device Name: | ACCUCON |
| Classification | Lens, Contact (other Material) - Daily |
| Applicant | INNOVISION, INC. 3125 SOUTH 61ST AVE. Omaha, NE 68106 -3675 |
| Contact | Don M Woodford |
| Correspondent | Don M Woodford INNOVISION, INC. 3125 SOUTH 61ST AVE. Omaha, NE 68106 -3675 |
| Product Code | HQD |
| CFR Regulation Number | 886.5916 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-30 |
| Decision Date | 1994-12-07 |
Trademark Results [ACCUCON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ACCUCON 86563522 4850049 Live/Registered |
Innovision, Inc. 2015-03-13 |
 ACCUCON 72448056 0983302 Dead/Cancelled |
PRECISION OPTICS, INC. 1973-03-01 |
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