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

The Nanostim Introducer Kit

K Number: K160716 · Decision Apr 14, 2016
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
23
Review Days
30

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Basic Information

Device Name
The Nanostim Introducer Kit
K Number
K160716
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
St. Jude Medical, Inc.
Date Received
March 15, 2016
Decision Date
April 14, 2016
Product Code
DYB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DYB Introducer, Catheter

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Other Clearances by St. Jude Medical, Inc.

K Number Device Name
K172393 Advisor HD Grid Mapping Catheter, Sensor Enabled
K163407 Confirm Rx Insertable Cardiac Monitor (ICM) System
K161171 PressureWire X Guidewire
K161102 Nanostim Introducer Kit
K140793 NANOSTIM INTRODUCER KIT
K133481 SJM CONFIRM IMPLANTABLE CARDIAC MONITOR (ICM)
K131592 ENLIGHTN RENAL GUIDE CATHETER
K073700 6F PROXIS SYSTEM
K042734 SJM RIGID SADDLE RING MODEL RSAR-(SIZE)
K022363 SJM TAILOR ANNULOPLASTY BAND, MODEL TAB-(SIZE) (TAILOR BAND)
Search all 23 clearances from St. Jude Medical, Inc. →