Deseret(R) Introducer Set with Vitacuff(R) Device

by Bd Becton Dickinson Vacutainer Systems Preanalytic 510(k)

Active United States

510(k) K893126

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESD Substantially Equivalent — Deferred · Traditional	NumberK893126	Date10 Aug 1989Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K893126
FDA Product Code: LJS

Device Class: Class II
Regulation: 21 CFR Part 880.5970
Advisory Committee: General Hospital
FDA Decision: SESD Substantially Equivalent — Deferred

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