Disposable Flush Device

by Hewlett-Packard Co. 510(k)

Active United States

510(k) K860681

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK860681	Date17 Jun 1986Cleared	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Withdrawn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: K860681
FDA Product Code: DRS

Device Class: Class II
Regulation: 21 CFR Part 870.2850
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

Other devices from Hewlett-Packard Co.

Luer Lock Skirt

Class II
Hp Sonos 100 Cf Ultrasound Imaging System

Class II
Medical Diag. Ultrasound Instr. 77065

Class II
Model M1403A Telemetry Monitoring Systems (TMS)

Class II
Differential Refractive Index Detector

Class I
Model 80100A, Patient Data Memory

Class II

See all devices from Hewlett-Packard Co. →