FDA 510(k) Applications Submitted by LONGPORT, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990238 | 01/25/1999 | LONGPORT MODEL LDS -1 | LONGPORT, INC. |
| K062571 | 08/31/2006 | LONGPORT EPISCAN, MODEL-I-200 | LONGPORT, INC. |
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