# K980751: Sabratek 4040 Infusion Pump

- Pathway: 510(k) (Traditional)
- Applicant: Sabratek Corp.
- Decided: Feb 24, 1999 after 363 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K914589 (1992). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K941984: Sabratek 6060 Homerun Volumetric Infusion Pump, Sabratek Corp. (1994) Summary page 1.
- K914589: Sabratek 3030 Infusion Pump, Sabratek Corp. (1992). Our OCR of the scanned summary read K914581, FDA’s number for Heart Technology Wireclip (Heart Technology, Inc.). Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “Sabratek 3030 Infusion Pump”.

## Indications for use
Provide controlled delivery of fluids, blood and blood products and can be used in enteral, epidural, subcutancous, arterial and intravenous applications.

Source page: https://510kreport.com/device/K980751
Methodology: https://510kreport.com/methodology