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NOVOFLO CATHETER LT

Page Type
Cleared 510(K)
510(k) Number
K072499
510(k) Type
Traditional
Applicant
NOVOSCI, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/30/2007
Days to Decision
55 days
Submission Type
Summary

NOVOFLO CATHETER LT

Page Type
Cleared 510(K)
510(k) Number
K072499
510(k) Type
Traditional
Applicant
NOVOSCI, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/30/2007
Days to Decision
55 days
Submission Type
Summary