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

TAUT-INSUFFLATION NEEDLE

K Number: K003703 · Decision Feb 22, 2001
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
16
Review Days
83

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Basic Information

Device Name
TAUT-INSUFFLATION NEEDLE
K Number
K003703
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Taut, Inc.
Date Received
December 1, 2000
Decision Date
February 22, 2001
Product Code
HIF
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIF Insufflator, Laparoscopic

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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
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
K945486 SPLATTER CONTROL SHIELD
Search all 16 clearances from Taut, Inc. →