Cardiometrics Flowire Doppler Guide Wire

by Cardio Metrics, Inc. 510(k)

Active United States

510(k) K943022

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK943022	Date19 Sep 1994Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
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: K943022
FDA Product Code: DQX

Device Class: Class II
Regulation: 21 CFR Part 870.1330
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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