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EZCHEK/HBA BLOOD COLLECTION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971919
510(k) Type
Traditional
Applicant
FLEXSITE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1997
Days to Decision
105 days
Submission Type
Summary

EZCHEK/HBA BLOOD COLLECTION KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971919
510(k) Type
Traditional
Applicant
FLEXSITE DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/1997
Days to Decision
105 days
Submission Type
Summary