Cardio-Slidecomp

by Creative Instruments

510(k) K790869

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K790869↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK790869	Date17 May 1979Cleared	StatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K790869
FDA Product Code: DPS

Device Class: Class II
Regulation: 21 CFR Part 870.2340
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

Overview

AI-generated summary, 23 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The CARDIO-SLIDECOMP is a cardiovascular device. It is identified by the device name CARDIO-SLIDECOMP and product code DPS.

It received traditional 510(k) clearance from the FDA under K790869 on May 17, 1979, following a determination of substantial equivalence. The device was reviewed by the Cardiovascular advisory committee.