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HemosIL ReadiPlasTin

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213426
510(k) Type
Traditional
Applicant
Instrumentation Laboratory Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2022
Days to Decision
299 days
Submission Type
Summary

HemosIL ReadiPlasTin

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213426
510(k) Type
Traditional
Applicant
Instrumentation Laboratory Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2022
Days to Decision
299 days
Submission Type
Summary