510(k) K950485

GRAPHIC CONTROLS PROTRACE ECG ELECTRODE by Graphic Controls Corp. — Product Code DRX

K950485 is an FDA 510(k) premarket notification submitted by Graphic Controls Corp. for the device "GRAPHIC CONTROLS PROTRACE ECG ELECTRODE". The FDA issued a decision of Substantially Equivalent on July 7, 1995. The device falls under product code DRX (Electrode, Electrocardiograph), a Class II device regulated under 21 CFR 870.2360. Graphic Controls Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 7, 1995
Date Received
February 6, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Electrode, Electrocardiograph
Device Class
Class II
Regulation Number
870.2360
Review Panel
CV
Submission Type