Last synced on 14 November 2025 at 11:06 pm

Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17

Page Type
Cleared 510(K)
510(k) Number
K221616
510(k) Type
Traditional
Applicant
CAF Medical Solutions Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2022
Days to Decision
59 days
Submission Type
Summary

Patient Monitor, models LMPLUS-12, LMPLUS-15 and LMPLUS-17

Page Type
Cleared 510(K)
510(k) Number
K221616
510(k) Type
Traditional
Applicant
CAF Medical Solutions Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/2022
Days to Decision
59 days
Submission Type
Summary