510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950304Substantially Equivalent

Deseret (R) T-Port (R) Multi Flo(tm) and Deseret (R)prn Adapter

Becton Dickinson Vascular Access, Inc., Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K950304 is the FDA 510(k) clearance record for DESERET (R) T-PORT (R) MULTI FLO(TM) AND DESERET (R)PRN ADAPTER, a class II device, cleared for Becton Dickinson Vascular Access, Inc. on under FDA product code FPA (Set, Administration, Intravascular). FDA records list 25 510(k) clearances for Becton Dickinson Vascular Access, Inc., from to . As of , FDA records show no recalls naming K950304.

Clearance record

Decision date
Received
(48 days to decision)
Product code
FPA Set, Administration, Intravascular
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Becton Dickinson Vascular Access, Inc. 9450 S. State St., Sandy UT
510(k) summary
Summary
Third party review
No

Clearances, product code FPA

Trailing 12 months
5 clearances under product code FPA in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FPA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20261
October 20260