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Parenteral Infusion Controller, Elec.

by National Patent Development Corp.

510(k) K780106

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 6 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Regulatory status

as of registry sync 6 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK780106 Date21 Feb 1978ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 6 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  • Withdrawn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
FLN
Device Class
Class II
Regulation
21 CFR Part 880.2420
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 24 Sep 2026

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

The Parenteral Infusion Controller, Elec. is a medical device classified as a Monitor, Electric For Gravity Flow Infusion Systems. It is designed to control the infusion of parenteral medications or fluids through gravity flow systems.

This device is manufactured by National Patent Development Corp. and is supplied as a reusable device. It received FDA 510(k) clearance with number K780106 on February 21, 1978, and is classified under product code FLN with regulation number 880.2420.

Other devices from National Patent Development Corp.

See all devices from National Patent Development Corp. →

Questions

AI-generated answers, 24 Sep 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 Parenteral Infusion Controller Elec used for?

    The Parenteral Infusion Controller, Elec is designed to control the infusion of parenteral medications or fluids through gravity flow systems. It serves as an electric monitor to ensure accurate and controlled administration of fluids in medical settings.

  • Is this device reusable or single-use?

    The Parenteral Infusion Controller, Elec is supplied as a reusable device. It is designed for multiple uses in clinical settings, though proper cleaning and maintenance protocols should be followed between uses to ensure proper functionality and patient safety.

  • What regulatory approvals does this device have?

    This device received FDA 510(k) clearance with number K780106 on February 21, 1978. It is classified under product code FLN with regulation number 880.2420 and is considered substantially equivalent to predicate devices.

  • What sizes or models of this infusion controller are available?

    The device data does not specify different sizes or models of the Parenteral Infusion Controller, Elec. The information provided indicates a single device type manufactured by National Patent Development Corp. for use with gravity flow infusion systems.