FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTRADUCER

K Number: K921934 · Decision Jul 15, 1992
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
16
Review Days
82

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Basic Information

Device Name
INTRADUCER
K Number
K921934
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Taut, Inc.
Date Received
April 24, 1992
Decision Date
July 15, 1992
Product Code
GBX
Advisory Committee
General, Plastic Surgery
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
GBX Catheter, Irrigation

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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
K960883 INTRADUCER PERITONEAL CATHETER 6FRX3, 9FRX3 1/2, 10FRX4, 12FRX8
Search all 16 clearances from Taut, Inc. →