Last synced on 14 November 2025 at 11:06 pm

R&D HGB/GLC WHOLE BLOOD CONTROL

Page Type
Cleared 510(K)
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)
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