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RE1000 HEART RATE MONITOR

Page Type
Cleared 510(K)
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)
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