FDA 510(k) Applications Submitted by CATHY ANNE PINTO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K955389 | 11/24/1995 | MR GUIDED PROCEDURES PACKAGE/MAGNETOM OPEN SYSTEM | SIEMENS MEDICAL SOLUTIONS USA, INC. |
| K961121 | 03/21/1996 | KINEMATIC KNEE DEVICE/MAGNETOM OPEN SYSTEM | SIEMENS MEDICAL SOLUTIONS USA, INC. |
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