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MEDIGARD BLOOD COLLECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082511
510(k) Type
Traditional
Applicant
MEDIGARD LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
140 days
Submission Type
Summary

MEDIGARD BLOOD COLLECTION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K082511
510(k) Type
Traditional
Applicant
MEDIGARD LIMITED
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/16/2009
Days to Decision
140 days
Submission Type
Summary