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R&D HGB/GLC WHOLE BLOOD CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993321
510(k) Type
Traditional
Applicant
R & D SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1999
Days to Decision
39 days
Submission Type
Summary

R&D HGB/GLC WHOLE BLOOD CONTROL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993321
510(k) Type
Traditional
Applicant
R & D SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/12/1999
Days to Decision
39 days
Submission Type
Summary