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BIOMONITOR IIIm, BIOMONITOR III

Page Type
Cleared 510(K)
510(k) Number
K221856
510(k) Type
Special
Applicant
BIOTRONIK, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2022
Days to Decision
30 days
Submission Type
Summary

BIOMONITOR IIIm, BIOMONITOR III

Page Type
Cleared 510(K)
510(k) Number
K221856
510(k) Type
Special
Applicant
BIOTRONIK, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/27/2022
Days to Decision
30 days
Submission Type
Summary