# K002191: Carriazo Barraquer II Microkeratome

- Pathway: 510(k) (Traditional)
- Applicant: Moria, Inc.
- Decided: Oct 12, 2000 after 84 days
- Product code: HMY (Keratome, Battery-Powered)
- Device class: 1
- Regulation: 21 CFR 886.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 7 cite it directly.
0 of 10 devices in its family (counting itself) have 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.

## Most influential descendants
- K040297: Oneuse- Plus Microkeratome (2004), 2 descendants of its own
- K043183: EPI-K (2005), 1 descendant of its own
- K030401: Disposable M2-PE Microkeratome Blades (2003), 1 descendant of its own
- K172994: EPI K Console (2017), 0 descendants of its own
- K041110: MB 105 Millennium Blades (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K002191
Methodology: https://510kreport.com/methodology