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LifeLens Wireless ECG Monitor

Page Type
Cleared 510(K)
510(k) Number
K203168
510(k) Type
Traditional
Applicant
LifeLens Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2021
Days to Decision
270 days
Submission Type
Summary

LifeLens Wireless ECG Monitor

Page Type
Cleared 510(K)
510(k) Number
K203168
510(k) Type
Traditional
Applicant
LifeLens Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/20/2021
Days to Decision
270 days
Submission Type
Summary