FDA 510(k) Applications Submitted by Lite-Med Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142561 | 09/11/2014 | LM-9300 ELMA Lithotripter | LITE-MED INC. |
| K213772 | 12/02/2021 | LM-9300 Plus Lithotripter | Lite-Med Inc. |
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