FDA 510(k) Applications Submitted by DAVID PUTZ

FDA 510(k) Number Submission Date Device Name Applicant
K990788 03/10/1999 AD-TECH'S FORAMEN OVALE ELECTRODE AD-TECH MEDICAL INSTRUMENT CORP.
K964644 10/31/1996 AD-TECH'S DEPTH ELECTRODE AD-TECH MEDICAL INSTRUMENT CORP.


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