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

MEDI-TRACE(R) 500 ECG ELECTRODE

K Number: K945479 · Decision Jul 7, 1995
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
55
Review Days
241

Basic Information

Device Name
MEDI-TRACE(R) 500 ECG ELECTRODE
K Number
K945479
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
GRAPHIC CONTROLS CORP.
Date Received
November 8, 1994
Decision Date
July 7, 1995
Product Code
DRX
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
DRX Electrode, Electrocardiograph

Similar 510(k) Clearances

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

View all

Other Clearances by GRAPHIC CONTROLS CORP.

K Number Device Name
K981964 MEDI-TRACE 4103 NEONATAL ELECTRODE
K983287 MEDI-TRACE 1610C COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODE
K974730 SOFTRANS PLUS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 5000, SOFTRANS PLUS IUPC)
K980857 MEDI-TRACE 1310P COMBINATION DEFIBRILLATION, MONITORING & PACING ELECTRODE
K972970 MEDI-TRACE 1510M COMBINATION DEFIBRILLATION, MONITORING AND PACING ELECTRODE
K964387 POINT OF USE II SHARPS-A-GATOR
K964279 SOFTRANS INTRAUTERINE PRESSURE CATHETER SYSTEM (IUP 4000 SOFTRANS IUPC)
K963151 MEDI-TRACE 5700 RESTING ECG ELECTRODE
K963038 MEDI-TRACE 3600 SERIES OF ECG MONITORING ELECTRODE
K960968 MEDI-TRACE 200, MEDI-TRACE 200-30
Search all 55 clearances from GRAPHIC CONTROLS CORP. →