# K113633: Mckesson Anesthesia Care

- Pathway: 510(k) (Traditional)
- Applicant: Mckesson Technologies, Inc.
- Decided: Apr 20, 2012 after 134 days
- Product code: BSZ (Gas-Machine, Anesthesia)
- Device class: 2
- Regulation: 21 CFR 868.5160
- Recalls of this device: 1 (1 Class I)
- 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.
1 of 1 device in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Mar 15, 2013 · Class I · Z-1060-2014: There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record (ACR) in that it included data from another case.

Source page: https://510kreport.com/device/K113633
Methodology: https://510kreport.com/methodology