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ANEMIAPRO SELF-SCREENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042379
510(k) Type
Traditional
Applicant
BIOSAFE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2004
Days to Decision
105 days
Submission Type
Summary

ANEMIAPRO SELF-SCREENER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042379
510(k) Type
Traditional
Applicant
BIOSAFE LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/15/2004
Days to Decision
105 days
Submission Type
Summary