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FDA 510(k)

AUTO SYRINGE(R) AS50 INFUSION PUMP

K-Number: K945942 · 1995-07-10

ApplicantBaxter Healthcare Corp
Decision Date1995-07-10
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

AUTO SYRINGE(R) AS50 INFUSION PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1995-07-10 under 510(k) number K945942. 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 AUTO SYRINGE(R) AS50 INFUSION PUMP?

AUTO SYRINGE(R) AS50 INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1995-07-10. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K945942.

When did AUTO SYRINGE(R) AS50 INFUSION PUMP receive FDA 510(k) clearance?

AUTO SYRINGE(R) AS50 INFUSION PUMP received FDA 510(k) clearance on 1995-07-10, under 510(k) number K945942.

Who is the listed applicant for AUTO SYRINGE(R) AS50 INFUSION PUMP?

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

What is the FDA product code for AUTO SYRINGE(R) AS50 INFUSION PUMP?

The FDA product code for AUTO SYRINGE(R) AS50 INFUSION PUMP is FRN.

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Other records listing Baxter Healthcare Corp as applicant

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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.

K253703RemunityPRO+ Pump for Remodulin® (treprostinil) InjectionDeka R&D CorpK252015FreedomEdge Infusion System; High-Flo SubQ Needle Set; Precision Flow Rate TubingKoru Medical Systems, Inc.K251636Spectrum IQ Infusion System with Dose IQ Safety Software (3570009)Baxter Healthcare CorporationK251640SIGMA Spectrum Infusion Pump with Master Drug LibraryBaxter Healthcare CorporationK242752MRidium 3870 MRI Infusion Pump System (3870)Iradimed CorporationK243855BD Alaris Infusion System with Guardrails Suite MXCarefusion 303, Inc.

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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