FDA 510(k) Applications Submitted by CLEMENT CLARKE INTL., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K980960 03/16/1998 IN-CHECK INSPIRATORY FLOWMETER CLEMENT CLARKE INTL., LTD.
K982334 07/02/1998 AIRZONE PEAK FLOWMETER CLEMENT CLARKE INTL., LTD.
K000368 02/04/2000 EYECAP IMAGING SYSTEM CLEMENT CLARKE INTL., LTD.
K962074 05/28/1996 VM PLUS PEAK FLOWMETER CLEMENT CLARKE INTL., LTD.
K042058 07/30/2004 ONEFLOW FVC, ONEFLOW FVC (KIT), ONEFLOW FVC SCREEN CLEMENT CLARKE INTL., LTD.
K053156 11/14/2005 MINI-WRIGHT DIGITAL, MODEL 3120001 CLEMENT CLARKE INTL., LTD.


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