The following data is part of a premarket notification filed by Vistech Consultants, Inc. with the FDA for Vcts 700s System.
Device ID | K881021 |
510k Number | K881021 |
Device Name: | VCTS 700S SYSTEM |
Classification | Chart, Visual Acuity |
Applicant | VISTECH CONSULTANTS, INC. 1372 NOTH FAIRFIELD RD. Dayton, OH 45432 |
Contact | Dennis J Mccreight |
Correspondent | Dennis J Mccreight VISTECH CONSULTANTS, INC. 1372 NOTH FAIRFIELD RD. Dayton, OH 45432 |
Product Code | HOX |
CFR Regulation Number | 886.1150 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-10 |
Decision Date | 1988-04-01 |