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

EP-4 CLINICAL STIMUTATOR

K Number: K041442 · Decision Sep 14, 2004
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
17
Applicant Total
12
Review Days
105

Basic Information

Device Name
EP-4 CLINICAL STIMUTATOR
K Number
K041442
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1750
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
EP MEDSYSTEMS
Date Received
June 1, 2004
Decision Date
September 14, 2004
Product Code
JOQ
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
JOQ Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JOQ), ordered by most recent decision date.

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Other Clearances by EP MEDSYSTEMS

K Number Device Name
K092913 EP-4TM CARDIAC STIMULATOR, MODELS: EP-04-02, EP-04-04
K073709 MODIFICATION TO VIEWMATE SYSTEM
K071028 VIEWMATE SYSTEM
K070706 EP-WORKMATE
K063113 EP-WORKMATE
K040207 EP-4 CLINICAL STIMULATOR
K031066 VIEWMATE ULTRASOUND IMAGING SYSTEM
K032225 EP-WORKMATE WITH RPM SYSTEM
K991001 MODIFICATION OF PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER
K984150 PROCATH ELECTROPHYSIOLOGY CATHETER, EP MEDSYSTEMS ELECTROPHYSIOLOGY CATHETER
Search all 12 clearances from EP MEDSYSTEMS →