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FDA 510(k)

ABC SYRINGE INFUSION PUMP, MODEL 4100

K-Number: K072603 · 2008-10-23

ApplicantElixir Corporation
Decision Date2008-10-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ABC SYRINGE INFUSION PUMP, MODEL 4100 is the device name listed in this FDA 510(k) record. The listed applicant is Elixir Corporation. It received FDA 510(k) clearance on 2008-10-23 under 510(k) number K072603. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABC SYRINGE INFUSION PUMP, MODEL 4100?

ABC SYRINGE INFUSION PUMP, MODEL 4100 is a medical device that received FDA 510(k) clearance on 2008-10-23. The listed applicant is Elixir Corporation. The 510(k) number is K072603.

When did ABC SYRINGE INFUSION PUMP, MODEL 4100 receive FDA 510(k) clearance?

ABC SYRINGE INFUSION PUMP, MODEL 4100 received FDA 510(k) clearance on 2008-10-23, under 510(k) number K072603.

Who is the listed applicant for ABC SYRINGE INFUSION PUMP, MODEL 4100?

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

What is the FDA product code for ABC SYRINGE INFUSION PUMP, MODEL 4100?

The FDA product code for ABC SYRINGE INFUSION PUMP, MODEL 4100 is FRN.

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Related Devices (Code: FRN)

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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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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