FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8

K Number: K960883 · Decision Mar 20, 1996
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
16
Review Days
15

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Basic Information

Device Name
INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8
K Number
K960883
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Taut, Inc.
Date Received
March 5, 1996
Decision Date
March 20, 1996
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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Other Clearances by Taut, Inc.

K Number Device Name
K023261 ADAPT BALLOON OPEN ACCESS PORT, MODEL 41244
K021731 ADAPT OPEN ACCESS PORT, MODEL 41233
K011018 TAUT BALLOON CATHETER, MODEL 50640
K003703 TAUT-INSUFFLATION NEEDLE
K010007 ADAPT LAPAROSCOPIC PORT & ADAPT REDUCER CAP
K992904 MINI-PORT
K992907 INTRADUCER
K972112 INTRADUCER PORT SC CATALOG#31275,31035,30915, AND 31450
K962003 TUAT SPLATTER CONTROL SHIELD SCS-300
K945486 SPLATTER CONTROL SHIELD
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