FDA 510(k) Applications Submitted by KRIS TEICH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963328 | 08/23/1996 | AMS AMBICOR PENILE PROSTHESIS | AMERICAN MEDICAL SYSTEMS, INC. |
| K030019 | 01/03/2003 | MODIFICATION TO HI-TORQUE WHISPER GUIDEWIRE | GUIDANT CORP. |
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