FDA 510(k) Applications Submitted by GLENN 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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