# K973851: Alexander Manufacturing CO. Rechargeable Battery #M12/630

- Pathway: 510(k) (Traditional)
- Applicant: Alexander Mfg. Co.
- Decided: Jan 5, 1998 after 89 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 K790373 (1979). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K790373: Ivac 630 Volumetric Infusion Pump, Y (1979) Summary page 3.

## Indications for use
Replacement battery for IVAC Corp. 125053 630 Volumetric Infusion Pump, Infu-Check #1500, 510(k) Number K790373. This battery is shipped only to customers who request a replacement battery for a particular device or to replace a competitor’s replacement battery. The biomedical equipment technician therefore knows the intended use is as a replacement battery.

Source page: https://510kreport.com/device/K973851
Methodology: https://510kreport.com/methodology