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Technitex, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K893968
VKG 2000 VIDEO KERATOMETER
September 11, 1989
K883471
VKG 1000, VIDEO KERATOMETER
November 8, 1988
K882902
QRK 100, QUALITATIVE RING KERATOSCOPE
August 4, 1988