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FDA 510(k) Applications Submitted by GLENN D YEIK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050412
02/18/2005
VAPORMAX
TRIMEDYNE, INC.
K041660
06/18/2004
TRIMEDYNE HOLMIUM LASER SYSTEMS
TRIMEDYNE, INC.
K043012
11/02/2004
OMNIPULSE MINI, MODEL 2120
TRIMEDYNE, INC.
K022655
08/09/2002
TRIMEDYNE SIDE FIRING NEEDLE WITH VENT SHEATH
TRIMEDYNE, INC.
K053457
12/13/2005
VAPORMAX II
TRIMEDYNE, INC.
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