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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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