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

MEL-16-1, MEL-16-3 & MEL-16-5 TDK ECG ELECTRODES

K Number: K863369 · Decision Jan 6, 1987
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
6
Review Days
166

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MEL-16-1, MEL-16-3 & MEL-16-5 TDK ECG ELECTRODES
K Number
K863369
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Tdk Corp.
Date Received
July 24, 1986
Decision Date
January 6, 1987
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 Tdk Corp.

K Number Device Name
K883643 TDK ECG ELECTRODE, MEL-10L
K882904 TDK ELECTRODE MEL-20-1, MEL-20-3, MEL-20-5
K870834 TDK ECG ELECTRODE MEL-10
K854596 TDK ECG ELECTRODE MEL-08-09 & -11
K833899 TDK ECG ELECTRODE MEL-08