FDA 510(k) Applications Submitted by NUCLEAR ASSOC., DIV. INOVISION LP
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010417 | 02/12/2001 | CAL/RAD MARK IV-DOSE CALIBRATOR 34-162 VEENSTRA MODEL # VDC-304 | NUCLEAR ASSOC., DIV. INOVISION LP |
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