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)

MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES

K-Number: K884097 · 1989-04-17

ApplicantCircon Acmi
Decision Date1989-04-17
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES is the device name listed in this FDA 510(k) record. The listed applicant is Circon Acmi. It received FDA 510(k) clearance on 1989-04-17 under 510(k) number K884097. The device is classified under product code ODC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES?

MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1989-04-17. The listed applicant is Circon Acmi. The 510(k) number is K884097.

When did MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES receive FDA 510(k) clearance?

MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES received FDA 510(k) clearance on 1989-04-17, under 510(k) number K884097.

Who is the listed applicant for MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES?

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

What is the FDA product code for MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES?

The FDA product code for MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES is ODC.

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 Circon Acmi 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.

K013165USA SERIES LAPAROSCOPESK980492AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)K905705LAP 3501 HIGH FLOW INSUFFLATORK905706GYN-1500 HYSTEROSCOPIC INUFFLATORK884025CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200K884254CIRCON ACMI BICAP III THERAPEUTIC SYSTEM

View all 10 devices →

Related Devices (Code: ODC)

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.

K252933DYNE PORTDyne Medical Group, Inc.K250145Biopsy Port AdapterEndosound, Inc.K252910Orca Air/Water and Suction ValvesBoston ScientificK250949Suction Valve (MAJ-1443); Air/Water Valve (MAJ-1444)Olympus Medical Systems CorporationK250732Disposable Endoscopy Valve SetYangzhou Fartley Medical Instrument Technology Co., Ltd.K241842Luer-Split MAJ-2092Olympus Medical Systems Corporation

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.

↑