FDA 510(k) Applications Submitted by Inter-Med, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K221811 06/22/2022 Vista BC Sealer Inter-Med, Inc.
K211721 06/04/2021 PS System Inter-Med, INC.
K082470 08/27/2008 SODIUM HYPOCHLORITE 3 & 6% SOLUTION AND 6% WITH WETTING AGENTS TO LOWER SURFACE TENSION MARKETED AS CHLOR-XTRA INTER-MED, INC.
K112250 08/04/2011 CHX=CHX PLUS INTER-MED, INC.


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