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VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification Kit

Page Type
Cleared 510(K)
510(k) Number
K153712
510(k) Type
Traditional
Applicant
Radiometer America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
35 days
Submission Type
Summary

VK-3 Verification Kit, VK-4 Verification Kit, VK-R5 Verification Kit, VK-R7 Verification Kit, VK-Crea Verification Kit

Page Type
Cleared 510(K)
510(k) Number
K153712
510(k) Type
Traditional
Applicant
Radiometer America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
35 days
Submission Type
Summary