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

PRE VUE

K Number: K830573 · Decision Mar 29, 1983
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
16
Review Days
34

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Basic Information

Device Name
PRE VUE
K Number
K830573
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5200
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Taut, Inc.
Date Received
February 23, 1983
Decision Date
March 29, 1983
Product Code
FOZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

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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. →