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

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER ACCESSORY CABLES

K Number: K030005 · Decision Mar 18, 2003
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
104
Applicant Total
33
Review Days
75

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Basic Information

Device Name
VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETER ACCESSORY CABLES
K Number
K030005
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vanguard Medical Concepts, Inc.
Date Received
January 2, 2003
Decision Date
March 18, 2003
Product Code
DSA
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
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

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Other Clearances by Vanguard Medical Concepts, Inc.

K Number Device Name
K053051 VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
K051616 VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
K051180 VANGUARD REPROCESSED EXTERNAL FIXATION DEVICES
K051043 VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS
K050763 VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS
K043198 VANGUARD REPROCESSED ARTHROSCOPIC WANDS
K043253 VANGUARD REPROCESSED DILATING TIP AND BLUNT TROCARS
K043594 VANGUARD REPROCESSED BLADED TROCAR, NON-BLADED TROCAR, TROCAR ACCESSORIES
K043225 VANGUARD REPROCESSED ULTRASONIC SCALPEL
K043315 VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL
Search all 33 clearances from Vanguard Medical Concepts, Inc. →