FDA 510(k) Applications Submitted by ROBERT N BORGHESE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960749 | 02/23/1996 | HEMOCHRON JR. MICROCOAGULATION LOW RANGE ACT | INTERNATIONAL TECHNIDYNE CORP. |
| K961835 | 05/13/1996 | PROTIME MICROCOAGULATION SYSTEM | INTERNATIONAL TECHNIDYNE CORP. |
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