FDA 510(k) Applications Submitted by ENCOMPASS GROUP, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K982058 06/11/1998 ROTECNO FR (FLUID RESISTANT) SURGICAL GOWN ENCOMPASS GROUP, LLC.
K982059 06/11/1998 ROTECNO 2000 SURGICAL GOWN ENCOMPASS GROUP, LLC.


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