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MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053571
510(k) Type
Traditional
Applicant
INTERLAB S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2006
Days to Decision
190 days
Submission Type
Statement

MICROGEL ALKALINE HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM, MICROGEL ACID HEMOGLOBIN ELECTROPHORESIS TEST SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053571
510(k) Type
Traditional
Applicant
INTERLAB S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2006
Days to Decision
190 days
Submission Type
Statement