# K132276: Sterile Empty Glass Container, 250ML, Sterile Empty Glass Container, 500 ML, Sterile Empty Glass Container, 1000 ML

- Pathway: 510(k) (Traditional)
- Applicant: Hospira, Inc.
- Decided: Nov 12, 2013 after 113 days
- Product code: KPE (Container, I.V.)
- Device class: 2
- Regulation: 21 CFR 880.5025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Empty Evacuated Container (Pre-amendment Device): named in the summary without a submission number

## Indications for use
The Hospira Sterile Empty Glass Container is indicated for admixing of compatible medications.

Source page: https://510kreport.com/device/K132276
Methodology: https://510kreport.com/methodology