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FDA 510(k)

NIPRO SUREFUSER AMBULATORY INFUSION PUMP

K-Number: K051828 · 2005-12-15

ApplicantNipro Medical Corporation
Decision Date2005-12-15
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NIPRO SUREFUSER AMBULATORY INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Nipro Medical Corporation. It received FDA 510(k) clearance on 2005-12-15 under 510(k) number K051828. The device is classified under product code MEB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NIPRO SUREFUSER AMBULATORY INFUSION PUMP?

NIPRO SUREFUSER AMBULATORY INFUSION PUMP is a medical device that received FDA 510(k) clearance on 2005-12-15. The listed applicant is Nipro Medical Corporation. The 510(k) number is K051828.

When did NIPRO SUREFUSER AMBULATORY INFUSION PUMP receive FDA 510(k) clearance?

NIPRO SUREFUSER AMBULATORY INFUSION PUMP received FDA 510(k) clearance on 2005-12-15, under 510(k) number K051828.

Who is the listed applicant for NIPRO SUREFUSER AMBULATORY INFUSION PUMP?

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

What is the FDA product code for NIPRO SUREFUSER AMBULATORY INFUSION PUMP?

The FDA product code for NIPRO SUREFUSER AMBULATORY INFUSION PUMP is MEB.

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Other records listing Nipro Medical Corporation as applicant

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Related Devices (Code: MEB)

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.

K250234SMARTeZ™ Elastomeric Infusion Pump (RS series)Epic Medical Pte. , Ltd.K240624InfuLifeFirst Medical Source, LLCK242152SMARTeZ™ Elastomeric Infusion Pump (498111, 498121, 498131, 498141)Epic Medical Pte. , Ltd.K181360ON-Q* Pump with BolusHalyard HealthK151650SMARTez elastomeric infusion pumpEpic Medical Pte. , Ltd.K131247MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEMMfs - Medical Flow Systems, 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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