FDA 510(k) Applications Submitted by LOUIS M. GERSON CO., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960778 | 02/26/1996 | ISOLAIR APR TYPE N95 | LOUIS M. GERSON CO., INC. |
| K050193 | 01/27/2005 | GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR | LOUIS M. GERSON CO., INC. |
| K061375 | 05/17/2006 | RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 | LOUIS M. GERSON CO., INC. |
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