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RE1000 HEART RATE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822319
510(k) Type
Traditional
Applicant
ELECTRONIC MONITORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
42 days

RE1000 HEART RATE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822319
510(k) Type
Traditional
Applicant
ELECTRONIC MONITORS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/14/1982
Days to Decision
42 days