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NOVOFLO CATHETER LT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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