FDA 510(k) Applications Submitted by CAROLYN M STEELE-HUSTEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971527 | 04/28/1997 | INNOSENSE PELVIC FLOOR STIMULATION AND ELECTROMYOGRAPHY SYSTEM | EMPI |
| K962646 | 07/08/1996 | PRIME MODULAR ENDO HEAD | ORTHOPAEDIC INNOVATIONS, INC. |
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