510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924737Substantially Equivalent

Innersense(tm) Disposable Microtransducer

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

K924737 is the FDA 510(k) clearance record for INNERSENSE(TM) DISPOSABLE MICROTRANSDUCER, a class II device, cleared for Becton Dickinson Vascular Access, Inc. on under FDA product code DXO (Transducer, Pressure, Catheter Tip). FDA records list 25 510(k) clearances for Becton Dickinson Vascular Access, Inc., from to . As of , FDA records show no recalls naming K924737.

Clearance record

Decision date
Received
(335 days to decision)
Product code
DXO Transducer, Pressure, Catheter Tip
Regulation
21 CFR 870.2870
Device class
Class II
Review panel
Cardiovascular
Applicant
Becton Dickinson Vascular Access, Inc. 9450 S. State St., Sandy UT
510(k) summary
Summary
Third party review
No

Clearances, product code DXO

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