Last synced on 14 November 2025 at 11:06 pm

DISPOSABLE ECG MONITORING ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K950473
510(k) Type
Traditional
Applicant
NIKOMED U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1995
Days to Decision
312 days
Submission Type
Statement

DISPOSABLE ECG MONITORING ELECTRODE

Page Type
Cleared 510(K)
510(k) Number
K950473
510(k) Type
Traditional
Applicant
NIKOMED U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/12/1995
Days to Decision
312 days
Submission Type
Statement