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FDA 510(k)

SYRINGE PUMP 209-100

K-Number: K822454 · 1982-10-18

ApplicantMedix Corp.
Decision Date1982-10-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE PUMP 209-100 is the device name listed in this FDA 510(k) record. The listed applicant is Medix Corp.. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822454. 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 SYRINGE PUMP 209-100?

SYRINGE PUMP 209-100 is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Medix Corp.. The 510(k) number is K822454.

When did SYRINGE PUMP 209-100 receive FDA 510(k) clearance?

SYRINGE PUMP 209-100 received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822454.

Who is the listed applicant for SYRINGE PUMP 209-100?

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

What is the FDA product code for SYRINGE PUMP 209-100?

The FDA product code for SYRINGE PUMP 209-100 is FRN.

Related Clinical Trials

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Other records listing Medix Corp. 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.

K921273EASIMIST ULTRASONIC NEBULIZERK914772MEDIX NEBULIZING SYSTEM CODE NO. 2000 AND 2001K853071MEDIX ELECTRONIC NEBULIZING SYSTEMK780444NERVTRON-RX

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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