Parenteral Infusion Controller, Elec.
by National Patent Development Corp.
510(k) K780106
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK780106 | Date21 Feb 1978 | StatusActive |
Recalls
No FDA recalls found in the data synced 6 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 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
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.
Questions
AI-generated answers, 24 Sep 2026
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.