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FDA 510(k)

DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM

K-Number: K072921 · 2007-11-26

ApplicantSymbios Medical Products, LLC
Decision Date2007-11-26
Product CodeMEB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Symbios Medical Products, LLC. It received FDA 510(k) clearance on 2007-11-26 under 510(k) number K072921. 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 DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM?

DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-26. The listed applicant is Symbios Medical Products, LLC. The 510(k) number is K072921.

When did DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM receive FDA 510(k) clearance?

DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM received FDA 510(k) clearance on 2007-11-26, under 510(k) number K072921.

Who is the listed applicant for DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM?

The FDA 510(k) record lists Symbios Medical Products, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM?

The FDA product code for DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM is MEB.

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 Symbios Medical Products, LLC 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.

K071735MODIFICATION TO DISPOSABLE INFUSION PUMP KITK051474SYMBIOS DISPOSABLE INFUSION PUMP KIT

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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