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FDA 510(k)

MODEL 2000 AMBULATORY MED. INFUSER

K-Number: K833723 · 1984-01-30

ApplicantParker Hannifin Corp.
Decision Date1984-01-30
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 2000 AMBULATORY MED. INFUSER is the device name listed in this FDA 510(k) record. The listed applicant is Parker Hannifin Corp.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K833723. 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 MODEL 2000 AMBULATORY MED. INFUSER?

MODEL 2000 AMBULATORY MED. INFUSER is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Parker Hannifin Corp.. The 510(k) number is K833723.

When did MODEL 2000 AMBULATORY MED. INFUSER receive FDA 510(k) clearance?

MODEL 2000 AMBULATORY MED. INFUSER received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833723.

Who is the listed applicant for MODEL 2000 AMBULATORY MED. INFUSER?

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

What is the FDA product code for MODEL 2000 AMBULATORY MED. INFUSER?

The FDA product code for MODEL 2000 AMBULATORY MED. INFUSER is FRN.

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Other records listing Parker Hannifin 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.

K161731Cleveland Multiport Ventricular Catheter SetK897086PARKER AMBULATORY MEDICATION INFUSION PUMP 2004K863532MODIFIED LABELING TO MODEL 2000 AMBULATORY INFUSERK834461INFUSION PUMP PRIMERK831402PRESSURE MONITOR & CONTROL UNIT APC-02AK831747PLASMA THERAPY TUBESET-E100 SERIES

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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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