The following data is part of a premarket notification filed by Innovision, Inc. with the FDA for Accucon.
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 |
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 |