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FDA 510(k)

FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE

K-Number: K090882 · 2010-04-23

ApplicantHospira, Inc.
Decision Date2010-04-23
Product CodeNGT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE is the device name listed in this FDA 510(k) record. The listed applicant is Hospira, Inc.. It received FDA 510(k) clearance on 2010-04-23 under 510(k) number K090882. The device is classified under product code NGT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE?

FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE is a medical device that received FDA 510(k) clearance on 2010-04-23. The listed applicant is Hospira, Inc.. The 510(k) number is K090882.

When did FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE receive FDA 510(k) clearance?

FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE received FDA 510(k) clearance on 2010-04-23, under 510(k) number K090882.

Who is the listed applicant for FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE?

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

What is the FDA product code for FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE?

The FDA product code for FLUSH SYRINGE FILLED WITH 0.9% SODIUM CHLORIDE is NGT.

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Other records listing Hospira, Inc. 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.

K161469Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play ModuleK161036Hospira Extension Set, Hospira Primary SetK160492Hospira Sapphire SetsK160870Hospira Administration SetsK143612LifeCare PCA Infusion SystemK132276STERILE EMPTY GLASS CONTAINER, 250ML, STERILE EMPTY GLASS CONTAINER, 500 ML, STERILE EMPTY GLASS CONTAINER, 1000 ML

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Related Devices (Code: NGT)

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.

K2508840.9 % Sodium Chloride Injection, USP, BD PosiFlush™ SP SyringeBecton, Dickinson and CompanyK233623Praxiject™ SP 0.9% NaClMedxl, Inc.K231724Flush Syringe (Prefilled 0.9% normal saline solution)Spm Medicare Pvt. , Ltd.K231363Hantech Pre-filled 0.9% Normal Saline Flush Syringes (Models PFS-1003, PFS-1005, PFS-1010)Hantech Medical Device Co., Ltd.K230756TK Pre-Filled Normal Saline Flush SyringeAnhui Tiankang Medical Technology Co., Ltd.K223584Pre-Filled Normal Saline Flush SyringeAnhui Tianyang Pharmaceutical Co., 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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