Last synced on 25 January 2026 at 3:41 am

VENIPUNCTURE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963070
510(k) Type
Traditional
Applicant
Miller Products and Services
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1996
Days to Decision
37 days
Submission Type
Statement

VENIPUNCTURE KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K963070
510(k) Type
Traditional
Applicant
Miller Products and Services
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/13/1996
Days to Decision
37 days
Submission Type
Statement