# K981412: M1145 (UPS1-1.25K-1G-MP) Ups

- Pathway: 510(k) (Traditional)
- Applicant: Clary Corp.
- Decided: Nov 23, 1998 after 217 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- 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 K870976 (1987). 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)
- K870976: Onguard 1000, Catalog #043611-000 & 043611-001, Cobe Laboratories, Inc. (1987) Summary page 1.

## Indications for use
This emergency power source accessory (UPS) is intended for use as a short-term emergency power source for ventilators, for hospital use only.

Source page: https://510kreport.com/device/K981412
Methodology: https://510kreport.com/methodology