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FDA 510(k)

NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE

K-Number: K051574 · 2005-08-26

ApplicantNipro Medical Corp.
Decision Date2005-08-26
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corp.. It received FDA 510(k) clearance on 2005-08-26 under 510(k) number K051574. 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 NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE?

NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE is a medical device that received FDA 510(k) clearance on 2005-08-26. The listed applicant is Nipro Medical Corp.. The 510(k) number is K051574.

When did NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE receive FDA 510(k) clearance?

NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE received FDA 510(k) clearance on 2005-08-26, under 510(k) number K051574.

Who is the listed applicant for NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE?

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

What is the FDA product code for NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE?

The FDA product code for NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE is FMF.

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Other records listing Nipro Medical Corp. 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.

K093985NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLEK081210NIPRO SAFETOUCH HUBER INFUSTION SETK072024NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634, 5M9693K063368NIPRO BIOHOLE NEEDLEK063721NIPRO SAFETOUCH II GAMMAK052474NIPRO HYPODERMIC NEEDLE

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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

View on FDA Database →

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

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