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FDA 510(k) Applications Submitted by MUNKTELL FILTER AB
FDA 510(k) Number
Submission Date
Device Name
Applicant
K014281
12/27/2001
GARD FILTER, COMBIGARD FILTE / HME
MUNKTELL FILTER AB
K014282
12/27/2001
BACSTOP FILTER,BACSTOP FILTER/HME
MUNKTELL FILTER AB
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