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FDA 510(k)

ACCUPRO ENTERAL FEEDING PUMP

K-Number: K841729 · 1984-06-01

ApplicantAmerican Mcgaw
Decision Date1984-06-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ACCUPRO ENTERAL FEEDING PUMP is the device name listed in this FDA 510(k) record. The listed applicant is American Mcgaw. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K841729. 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 ACCUPRO ENTERAL FEEDING PUMP?

ACCUPRO ENTERAL FEEDING PUMP is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is American Mcgaw. The 510(k) number is K841729.

When did ACCUPRO ENTERAL FEEDING PUMP receive FDA 510(k) clearance?

ACCUPRO ENTERAL FEEDING PUMP received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841729.

Who is the listed applicant for ACCUPRO ENTERAL FEEDING PUMP?

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

What is the FDA product code for ACCUPRO ENTERAL FEEDING PUMP?

The FDA product code for ACCUPRO ENTERAL FEEDING PUMP is FRN.

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Other records listing American Mcgaw 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.

K853549MCGAW/DROP WATCH FLOW MONITORK843639ADD-A-VIAL SOLUTION TRANSFER DEVICEK843954MIXING CONTAINERK840388PAB IV CONTAINERK840212CONCENTRATED PLATELET ADMIN. SETK831716CAPD - CATHETER ADAPTER

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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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