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EXACTRACE ADULT FOAM MONITORING ECG ELECTRODE CONMED MODEL 1510 AND INSTATRACE ADULT DIAPHORETIC FOAM ECG ELECTRODE CONM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963787
510(k) Type
Traditional
Applicant
Conmedcorp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
172 days
Submission Type
Statement

EXACTRACE ADULT FOAM MONITORING ECG ELECTRODE CONMED MODEL 1510 AND INSTATRACE ADULT DIAPHORETIC FOAM ECG ELECTRODE CONM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963787
510(k) Type
Traditional
Applicant
Conmedcorp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/11/1997
Days to Decision
172 days
Submission Type
Statement