Last synced on 25 January 2026 at 3:41 am

BIOMONITOR IIIm, BIOMONITOR III

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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