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Miami Eye Technology, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K841101CLAYMAN-PAREL CAPSULE COUPEURMay 16, 1984
K832912GELENDER VACUUM FIXATION RING SYSJanuary 10, 1984
K832996SURGICAL IOP MONITORNovember 28, 1983
K832997EPA AUTOMATED INFUSION POLEOctober 4, 1983
K832911ABBOTT GLOBE HOLDERSeptember 29, 1983
K831702RARE-EARTH INTRA-OCULAR MAGNETJune 30, 1983