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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