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DUAL LEAD (ECG1 & ECG2) ARRHYTHMIA ANALYSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920743
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1992
Days to Decision
202 days
Submission Type
Statement

DUAL LEAD (ECG1 & ECG2) ARRHYTHMIA ANALYSIS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920743
510(k) Type
Traditional
Applicant
NIHON KOHDEN AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/1992
Days to Decision
202 days
Submission Type
Statement