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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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