FDA 510(k) Applications Submitted by BOARD OF DIRECTORS, ALBERT BROWNE LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K971971 05/29/1997 BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK BOARD OF DIRECTORS, ALBERT BROWNE LTD.
K970918 03/12/1997 BROWNE STEAM INDICATOR BOARD OF DIRECTORS, ALBERT BROWNE LTD.


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