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MINICAP HEMOGLOBIN(E) KIT, MODEL 2207, 2227

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082227
510(k) Type
Traditional
Applicant
SEBIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2009
Days to Decision
231 days
Submission Type
Statement

MINICAP HEMOGLOBIN(E) KIT, MODEL 2207, 2227

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082227
510(k) Type
Traditional
Applicant
SEBIA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2009
Days to Decision
231 days
Submission Type
Statement