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MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
510(k) Number
K091386
510(k) Type
Special
Applicant
NUMIA MEDICAL TECHNOLOGY, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
144 days
Submission Type
Summary

MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
510(k) Number
K091386
510(k) Type
Special
Applicant
NUMIA MEDICAL TECHNOLOGY, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/2/2009
Days to Decision
144 days
Submission Type
Summary