Last synced on 14 November 2025 at 11:06 pm

HEMOSIL FACTOR VIII DEFICIENT PLASMA

Page Type
Cleared 510(K)
510(k) Number
K034007
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2004
Days to Decision
51 days
Submission Type
Summary

HEMOSIL FACTOR VIII DEFICIENT PLASMA

Page Type
Cleared 510(K)
510(k) Number
K034007
510(k) Type
Traditional
Applicant
INSTRUMENTATION LABORATORY CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2004
Days to Decision
51 days
Submission Type
Summary