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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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