FDA 510(k) Applications Submitted by KEN MOORE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K963505 | 09/03/1996 | TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM | TENET MEDICAL ENGINEERING |
| K963506 | 09/03/1996 | TENET RADIOLUCENT HAND TABLE | TENET MEDICAL ENGINEERING |
| K964102 | 10/11/1996 | TENET TIBIAL FRACTURE SUPPORT | TENET MEDICAL ENGINEERING |
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