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)

Defendo Fujifilm 700 Single Use Cleaning Adapter

K-Number: K250140 · 2025-02-20

ApplicantSteris Corparation
Decision Date2025-02-20
Product CodeODC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Defendo Fujifilm 700 Single Use Cleaning Adapter is the device name listed in this FDA 510(k) record. The listed applicant is Steris Corparation. It received FDA 510(k) clearance on 2025-02-20 under 510(k) number K250140. 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 Defendo Fujifilm 700 Single Use Cleaning Adapter?

Defendo Fujifilm 700 Single Use Cleaning Adapter is a medical device that received FDA 510(k) clearance on 2025-02-20. The listed applicant is Steris Corparation. The 510(k) number is K250140.

When did Defendo Fujifilm 700 Single Use Cleaning Adapter receive FDA 510(k) clearance?

Defendo Fujifilm 700 Single Use Cleaning Adapter received FDA 510(k) clearance on 2025-02-20, under 510(k) number K250140.

Who is the listed applicant for Defendo Fujifilm 700 Single Use Cleaning Adapter?

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

What is the FDA product code for Defendo Fujifilm 700 Single Use Cleaning Adapter?

The FDA product code for Defendo Fujifilm 700 Single Use Cleaning Adapter is ODC.

Other records listing Steris Corparation 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.

K213412VERIFY STEAM Integrating Indicator, VERIFY STEAM Integrating Indicator 5CM

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.

↑