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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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