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FDA 510(k)

DUOPROSS SYRINGES

K-Number: K042500 · 2005-02-22

ApplicantDuopross Meditech Corporation
Decision Date2005-02-22
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DUOPROSS SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Duopross Meditech Corporation. It received FDA 510(k) clearance on 2005-02-22 under 510(k) number K042500. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUOPROSS SYRINGES?

DUOPROSS SYRINGES is a medical device that received FDA 510(k) clearance on 2005-02-22. The listed applicant is Duopross Meditech Corporation. The 510(k) number is K042500.

When did DUOPROSS SYRINGES receive FDA 510(k) clearance?

DUOPROSS SYRINGES received FDA 510(k) clearance on 2005-02-22, under 510(k) number K042500.

Who is the listed applicant for DUOPROSS SYRINGES?

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

What is the FDA product code for DUOPROSS SYRINGES?

The FDA product code for DUOPROSS SYRINGES is FMF.

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.

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Other records listing Duopross Meditech Corporation 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.

K052445DUOPROSS NEEDLE

Related Devices (Code: FMF)

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.

K262581GraftGun Universal Graft Delivery System (GDS®)SurGenTec, LLCK252184SOL-M Luer Lock Syringe with Exchangeable Needle TraySol-Millennium Medical, Inc.K253747Disposable Pen Injector (KXYC-03C02, KXYC-03A03)Jiangsu Enjosim Medical Technology Co., Ltd.K260208Ultra-Fine™ SAFETY Insulin Syringeembecta Medical II, LLCK253110Sol-Glide Safety Needle; Sol-Glide Safety Needle with SyringeSol-Millennium Medical, Inc.K260514Profoject™ Safety Needle; Profoject™ Syringe with Safety Needle; Profoject™ Low Dead Space Syringe with Safety NeedleCMT Health PTE., Ltd.

Official Source

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

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