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)

IRRIGATION AND SUCTION APPARATUS

K-Number: K900430 · 1990-06-05

ApplicantAcorn Group, Inc.
Decision Date1990-06-05
Product CodeJCX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IRRIGATION AND SUCTION APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Acorn Group, Inc.. It received FDA 510(k) clearance on 1990-06-05 under 510(k) number K900430. 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 IRRIGATION AND SUCTION APPARATUS?

IRRIGATION AND SUCTION APPARATUS is a medical device that received FDA 510(k) clearance on 1990-06-05. The listed applicant is Acorn Group, Inc.. The 510(k) number is K900430.

When did IRRIGATION AND SUCTION APPARATUS receive FDA 510(k) clearance?

IRRIGATION AND SUCTION APPARATUS received FDA 510(k) clearance on 1990-06-05, under 510(k) number K900430.

Who is the listed applicant for IRRIGATION AND SUCTION APPARATUS?

The FDA 510(k) record lists Acorn Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IRRIGATION AND SUCTION APPARATUS?

The FDA product code for IRRIGATION AND SUCTION APPARATUS 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 Acorn Group, Inc. 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.

K914362TOP CERVICAL SPINE PLATES & TITANIUM BONE SCREWSK912905LARYNGOSCOPEK904126VISIRASER

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.

↑