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PC ARRHYTHMIA DETECTION/ANALYSIS - ARRHYTHMIA III

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860980
510(k) Type
Traditional
Applicant
SPACELABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1986
Days to Decision
71 days

PC ARRHYTHMIA DETECTION/ANALYSIS - ARRHYTHMIA III

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860980
510(k) Type
Traditional
Applicant
SPACELABS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/1986
Days to Decision
71 days