FDA 510(k) Applications Submitted by THE TIMETER GROUP

FDA 510(k) Number Submission Date Device Name Applicant
K871452 04/13/1987 CLASSIC (TM) 200 OXYGEN FLOWMETER THE TIMETER GROUP
K852374 06/04/1985 OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 THE TIMETER GROUP
K862171 06/09/1986 MP-500 ELECTRONIC NEBULIZER THE TIMETER GROUP
K844556 11/21/1984 KHM 2000 DRIP WATCHER THE TIMETER GROUP


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