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

STEREOTAXIS CATHETER ADVANCER SYSTEM

K Number: K021802 · Decision Apr 8, 2003
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
28
Review Days
309

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Basic Information

Device Name
STEREOTAXIS CATHETER ADVANCER SYSTEM
K Number
K021802
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stereotaxis, Inc.
Date Received
June 3, 2002
Decision Date
April 8, 2003
Product Code
DQY
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
DQY Catheter, Percutaneous

Similar 510(k) Clearances

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Other Clearances by Stereotaxis, Inc.

K Number Device Name
K253473 Synchrony
K251792 Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)
K250590 MAGiC Sweep™ EP Mapping Catheter
K193147 Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive System
K192775 Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and Cardiodri
K183027 Steerable catheter control system
K150312 Vdrive system, Vdrive Duo, Vdrive with V-Sono
K141530 VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CAS
K140804 VDRIVE WITH V-LOOP/ VDRIVE DUO
K133396 VDRIVE WITH V-SONO
Search all 28 clearances from Stereotaxis, Inc. →