Briox Model 2000-CA Compressor Unit

FDA 510(k) K791241 · Briox Technologies, Inc.

Substantially Equivalent

510(k) numberK791241

Submission

Device name
Briox Model 2000-CA Compressor Unit
Applicant
Briox Technologies, Inc.
Mchenry, IL, US
Received
July 6, 1979
Decision date
July 24, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JCX – Apparatus, Suction, Ward Use, Portable, Ac-Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

Other 510(k)s with product code JCX

510(k)DeviceApplicantDecision
K250964Protable Phlegm Suction Unit (JMA D01)JCX · Traditional Jiangsu Jumao X-Care Medical Equipment Co., Ltd.05/11/2026SE
K243638MV Flow Aspiration Pump (MVFLOWPMP01)JCX · Traditional Microvention06/13/2025SE
K251111CaryJCX · Traditional Excitus AS05/07/2025SE
K243418Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate TubingJCX · Special Micro Therapeutics, Inc. d/b/a ev3 Neurovascular12/02/2024SE
K233428Easycess Aspiration PumpJCX · Traditional Guangzhou Easycess Medical Co.,Ltd11/03/2023SE
K222552120V Neptune S Rover (0711-001-000);V2 4-Port Manifold (0750-400-000);V2 Specimen…JCX · Traditional Stryker Instruments12/09/2022SE
K182950Acare Suction UnitJCX · Traditional Acare Technology Co., Ltd.08/23/2019SE
K190789IntelliCartTM SystemJCX · Special Dornoch Medical Systems04/24/2019SE
K190105ZOOM Aspiration PumpJCX · Special Taiwan Biomaterial Co., Ltd.02/21/2019SE
K180115TWBM PumpJCX · Traditional Taiwan Biomaterial Co., Ltd.07/24/2018SE

More from Taiwan Biomaterial Co., Ltd.

510(k)DeviceDecision
K813507InfalertBZQ · Traditional 01/12/1982SE
K800078Briox Model-Aeromist · Traditional 02/05/1980SE
K791240Briox Model 2000-C Compressor UnitJCX · Traditional 07/24/1979SE
K791239Briox Model 2000-A Aspirator UnitJCX · Traditional 07/24/1979SE
K791238Briox Model 2000-CQ Quiet CompressorJCX · Traditional 07/24/1979SE

Questions and answers

When was Briox Model 2000-CA Compressor Unit cleared by the FDA?

Briox Model 2000-CA Compressor Unit (K791241) received a 510(k) decision of Substantially Equivalent on July 24, 1979, 18 days after the submission was received.

What is the product code of K791241?

The FDA product code is JCX – Apparatus, Suction, Ward Use, Portable, Ac-Powered, a Class II (moderate risk) device regulated under 21 CFR 878.4780.