Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMG MODEL SUA01 SUCTION UNIT

K-Number: K042349 · 2004-12-16

ApplicantEmg Technology Co., Ltd.
Decision Date2004-12-16
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EMG MODEL SUA01 SUCTION UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Emg Technology Co., Ltd.. It received FDA 510(k) clearance on 2004-12-16 under 510(k) number K042349. The device is classified under product code JCX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMG MODEL SUA01 SUCTION UNIT?

EMG MODEL SUA01 SUCTION UNIT is a medical device that received FDA 510(k) clearance on 2004-12-16. The listed applicant is Emg Technology Co., Ltd.. The 510(k) number is K042349.

When did EMG MODEL SUA01 SUCTION UNIT receive FDA 510(k) clearance?

EMG MODEL SUA01 SUCTION UNIT received FDA 510(k) clearance on 2004-12-16, under 510(k) number K042349.

Who is the listed applicant for EMG MODEL SUA01 SUCTION UNIT?

The FDA 510(k) record lists Emg Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMG MODEL SUA01 SUCTION UNIT?

The FDA product code for EMG MODEL SUA01 SUCTION UNIT is JCX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Emg Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K112421EMG SUCTION UNITK072634EMG TRITON -COMP,MODEL NCA01-XXX SERIESK063448EMG AC/DC SUCTION UNITK062888MIDDLE WHEEL DRIVE POWER CHAIR, CWD01K052438EMG HANDLE NEBULIZER NB02 SERIESK043520EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR

View all 11 devices →

Related Devices (Code: JCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250964Protable Phlegm Suction Unit (JMA D01)Jiangsu Jumao X-Care Medical Equipment Co., Ltd.K243638MV Flow Aspiration Pump (MVFLOWPMP01)MicroventionK251111CaryExcitus ASK243418Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate TubingMicro Therapeutics, Inc. d/b/a ev3 NeurovascularK233428Easycess Aspiration PumpGuangzhou Easycess Medical Co.,LtdK222552120V Neptune S Rover (0711-001-000);V2 4-Port Manifold (0750-400-000);V2 Specimen Collection Manifold Kit (0750-200-000);V2 Specimen Collection Tray (0750-210-000)Stryker Instruments

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑