FDA 510(k) Applications Submitted by BARRIERMED, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011446 05/11/2001 BARRIERPLUS POWDER-FREE SYNTHETIC POLYISOPRENE SURGICAL GLOVES BARRIERMED, INC.
K060733 03/20/2006 SYNTHALON PI POWDER-FREE SYNTHETIC POLYISOPRENE/POLYCHLOROPRENE EXAMINATION GLOVES MDL 1362-10 TO 1362-44 BARRIERMED, INC.


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