Last synced on 21 June 2024 at 11:04 pm

NAVIPRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020764
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
88 days
Submission Type
Summary

NAVIPRO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K020764
510(k) Type
Traditional
Applicant
KINAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2002
Days to Decision
88 days
Submission Type
Summary