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FDA 510(k) Applications Submitted by GLENN MILLER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K960883
03/05/1996
INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8
TAUT, INC.
K972112
06/05/1997
INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450
TAUT, INC.
K962003
05/22/1996
TUAT SPLATTER CONTROL SHIELD SCS-300
TAUT, INC.
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