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Inframed, 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
K864610
CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE
June 18, 1987
K852761
CILAS MODEL YM101
November 14, 1985
K844178
MODEL TT25RF
October 18, 1985