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MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
510(k) Number
K983321
510(k) Type
Special
Applicant
BAXA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1998
Days to Decision
14 days
Submission Type
Summary

MICROFUSE DUAL RATE INFUSER

Page Type
Cleared 510(K)
510(k) Number
K983321
510(k) Type
Special
Applicant
BAXA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/6/1998
Days to Decision
14 days
Submission Type
Summary