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FDA 510(k)

CORFLO 300 PUMP

K-Number: K944750 · 1995-06-19

ApplicantCorpak, Inc.
Decision Date1995-06-19
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent - Subject to Tracking & PMS

Device Summary

CORFLO 300 PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Corpak, Inc.. It received FDA 510(k) clearance on 1995-06-19 under 510(k) number K944750. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking & PMS.

Frequently Asked Questions

What is the CORFLO 300 PUMP?

CORFLO 300 PUMP is a medical device that received FDA 510(k) clearance on 1995-06-19. The listed applicant is Corpak, Inc.. The 510(k) number is K944750.

When did CORFLO 300 PUMP receive FDA 510(k) clearance?

CORFLO 300 PUMP received FDA 510(k) clearance on 1995-06-19, under 510(k) number K944750.

Who is the listed applicant for CORFLO 300 PUMP?

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

What is the FDA product code for CORFLO 300 PUMP?

The FDA product code for CORFLO 300 PUMP is FRN.

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 Corpak, Inc. 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.

K964514CORPAK MEDSYSTEMS CRUZ CATHETER FOR PERITONEAL DIALYSISK970178CLOG ZAPPER ENTERAL FEEDING TUBE DECLOGGING SYSTEM

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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