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)

ASPIRATION & IRRIGATION CATHETER

K-Number: K833331 · 1983-11-14

ApplicantMicrovasive
Decision Date1983-11-14
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ASPIRATION & IRRIGATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Microvasive. It received FDA 510(k) clearance on 1983-11-14 under 510(k) number K833331. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATION & IRRIGATION CATHETER?

ASPIRATION & IRRIGATION CATHETER is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Microvasive. The 510(k) number is K833331.

When did ASPIRATION & IRRIGATION CATHETER receive FDA 510(k) clearance?

ASPIRATION & IRRIGATION CATHETER received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833331.

Who is the listed applicant for ASPIRATION & IRRIGATION CATHETER?

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

What is the FDA product code for ASPIRATION & IRRIGATION CATHETER?

The FDA product code for ASPIRATION & IRRIGATION CATHETER is OCX.

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 Microvasive 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.

K872771LOW PROFILE GASTROSTOMYK870705THERMAL COAGULATORK861323REPLACEMENT GASTROSTOMY TUBEK861309JEJUNAL FEEDING TUBEK860366CHALLENGER HOT BIOPSY FORCEPSK860589INFLATOR/DEFLATOR PISTON SYRINGE

View all 18 devices →

Related Devices (Code: OCX)

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.

K251986AUXILIARY WATER TUBE MAJ-855Olympus Medical Systems CorporationK251997Single-Use Biopsy Valve (MAJ-1555)Olympus Medical Systems CorporationK242586ArgoCap (200.52)Ovesco Endoscopy AGK241704Endoscopic Water PumpHangzhou AGS MedTech Co., Ltd.K242357Water Container (MAJ-901); Water Container (MAJ-902)Olympus Medical Systems CorporationK241874Aspiration Catheter (2189)Hobbs Medical, Inc.

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.

↑