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Reichert Ophthalmic Instruments, Div. Leica, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K000288REICHERT CT200 CONTACT TONOMETERMarch 23, 2000
K964290EYECHEKJanuary 9, 1997
K941865XPERT NCTSeptember 29, 1994