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Lite-Med, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K213772LM-9300 Plus LithotripterJanuary 19, 2023
K142561LM-9300 ELMA LithotripterMarch 20, 2015
K103217LITE-MED LM-9200 ELMASeptember 28, 2011