Last synced on 25 January 2026 at 3:41 am

IV START KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963722
510(k) Type
Traditional
Applicant
Grand Medical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1996
Days to Decision
72 days
Submission Type
Statement

IV START KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963722
510(k) Type
Traditional
Applicant
Grand Medical Products
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/27/1996
Days to Decision
72 days
Submission Type
Statement