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NEEDLE/CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950574
510(k) Type
Traditional
Applicant
TRI-MED SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
2/24/1995
Days to Decision
28 days
Submission Type
Statement

NEEDLE/CANNULA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950574
510(k) Type
Traditional
Applicant
TRI-MED SPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
2/24/1995
Days to Decision
28 days
Submission Type
Statement