FDA 510(k) Applications Submitted by ADAM SPENCER CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K963092 08/08/1996 MAXI-TORQUE PLUS SOFTIP ANGIOGRAPHIC CATHETER ADAM SPENCER CORP.
K964331 10/30/1996 ASC HIGH PRESSURE BRAIDED TUBES ADAM SPENCER CORP.


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