Last synced on 25 January 2026 at 3:41 am

BIOMONITOR IV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230375
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2023
Days to Decision
95 days
Submission Type
Summary

BIOMONITOR IV

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K230375
510(k) Type
Traditional
Applicant
Biotronik, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2023
Days to Decision
95 days
Submission Type
Summary