FDA 510(k) Applications Submitted by MELLEN AIR MFG., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K961129 03/21/1996 AREMA II MELLEN AIR MFG., INC.
K963510 09/03/1996 APREMA I - ALTERNATING PRESSURE AIR FLOTATION MATTRESS SYSTEM MELLEN AIR MFG., INC.


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