# K945887: Precision Q I D Blood Glucose Test Strips

- Pathway: 510(k) (Traditional)
- Applicant: Medisense, Inc.
- Decided: Mar 23, 1995 after 112 days
- Product code: CGA (Glucose Oxidase, Glucose)
- Device class: 2
- Regulation: 21 CFR 862.1345
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
77 later devices descend from it; 6 cite it directly.
4 of 78 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K962295: Precision Qid Blood Glucose Test Strip (1996), 61 descendants of its own
- K963676: Precision G Blood Glucose Testing System (1997), 60 descendants of its own
- K971812: Precision Qid Blood Glucose Test Strip, Precision G Blood Glucose Test Strip (1997), 59 descendants of its own
- K983504: Precision Xtra Advanced Diabetes Management System, Precision Blood Glucose Test Strips, Precision Xtra B-Ketone Test ST (1999), 40 descendants of its own
- K970707: Elect II Blood Glucose Monitoring System (1997), 36 descendants of its own

Source page: https://510kreport.com/device/K945887
Methodology: https://510kreport.com/methodology