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FLUID LEVEL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K133870
510(k) Type
Traditional
Applicant
COLEMAN LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2014
Days to Decision
125 days
Submission Type
Summary

FLUID LEVEL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K133870
510(k) Type
Traditional
Applicant
COLEMAN LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/24/2014
Days to Decision
125 days
Submission Type
Summary