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/ Visidyne Corp.
Visidyne Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K811316
TRISCAN, MODELS 38,40,41,43 & 45
July 2, 1981
K810699
PANTOPS M-2 ELECTROPHYSIOLOGY SYSTEM
June 9, 1981
K810700
CHROMOPS FM-100 COLOR VISION TESTER
April 10, 1981