FDA 510(k) Applications Submitted by LIGHTHOUSE MEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960230 | 01/17/1996 | SNARE | LIGHTHOUSE MEDICAL, INC. |
| K960231 | 01/17/1996 | SPHINCTEROTOME | LIGHTHOUSE MEDICAL, INC. |
| K961049 | 03/15/1996 | FLEX NEEDLE | LIGHTHOUSE MEDICAL, INC. |
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