The following data is part of a premarket notification filed by Sensory Aids Corp. with the FDA for Viewscan.
Device ID | K863994 |
510k Number | K863994 |
Device Name: | VIEWSCAN |
Classification | Aid, Vision Image Intensification |
Applicant | SENSORY AIDS CORP. 205 WEST GRAND AVENUE, SUITE 122 Bensenville, IL 60106 |
Contact | Ron B Merrick |
Correspondent | Ron B Merrick SENSORY AIDS CORP. 205 WEST GRAND AVENUE, SUITE 122 Bensenville, IL 60106 |
Product Code | HOT |
CFR Regulation Number | 886.5910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-14 |
Decision Date | 1986-10-31 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VIEWSCAN 74408204 not registered Dead/Abandoned |
Ultima Electronics Corporation 1993-06-30 |
VIEWSCAN 73556474 1392588 Dead/Cancelled |
TEST MARKETING GROUP, THE 1985-09-03 |
VIEWSCAN 73387914 1275595 Dead/Cancelled |
WORMALD INTERNATIONAL SENSORY AIDSLIMITED9 BALFOUR TERRACECHRISTCHURCH NEW ZEALAND 1982-09-23 |