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Linshom Respiratory Monitoring Device (LRMD)

Page Type
Cleared 510(K)
510(k) Number
K190734
510(k) Type
Traditional
Applicant
Linshom Management LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2020
Days to Decision
315 days
Submission Type
Summary

Linshom Respiratory Monitoring Device (LRMD)

Page Type
Cleared 510(K)
510(k) Number
K190734
510(k) Type
Traditional
Applicant
Linshom Management LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2020
Days to Decision
315 days
Submission Type
Summary