FDA 510(k) Applications Submitted by PENLON LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K041076 04/26/2004 DELTA T PENLON LTD.
K960944 02/13/1996 PPV VAPORIZER (MODIFICATION) PENLON LTD.
K961468 04/17/1996 QUIK-FIL VAPORIZER KEYED FILLER PENLON LTD.
K010317 02/02/2001 AV 800 VENTILATOR PENLON LTD.
K010318 02/02/2001 PRIMA OXYGEN MONITOR PENLON LTD.
K002343 08/01/2000 SIGMA DELTA PENLON LTD.
K061102 04/19/2006 PRIMA ANAESTHESIA MACHINE PENLON LTD.


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