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AIM-V (R) MEDIUM, MODEL 087-0112

Page Type
Cleared 510(K)
510(k) Number
K022086
510(k) Type
Traditional
Applicant
Invitrogen Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2002
Days to Decision
179 days
Submission Type
Summary

AIM-V (R) MEDIUM, MODEL 087-0112

Page Type
Cleared 510(K)
510(k) Number
K022086
510(k) Type
Traditional
Applicant
Invitrogen Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2002
Days to Decision
179 days
Submission Type
Summary