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Accupro Enteral Feeding Pump

by American Mcgaw

510(k) K841729

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK841729 Date1 Jun 1984ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
FRN
Device Class
Class II
Regulation
21 CFR Part 880.5725
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Accupro Enteral Feeding Pump is an infusion pump designed for the delivery of enteral nutrition. It functions to regulate the flow of nutritional solutions to patients requiring enteral feeding support.

This device is classified under regulation number 880.5725 and is authorized for use via FDA 510(k) clearance. It is categorized within the General Hospital medical specialty.

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Questions

AI-generated answers, 6 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the primary function of the Accupro Enteral Feeding Pump?

    The Accupro Enteral Feeding Pump is an infusion pump designed to regulate the flow of nutritional solutions for patients who require enteral feeding support.

  • What is the regulatory status of this device?

    This device is classified under regulation number 880.5725 and is authorized for use via FDA 510(k) clearance.

  • In which medical specialty is this pump categorized?

    The device is categorized within the General Hospital medical specialty, as indicated by the advisory committee description.