# K896951: Satellite G Blood Glucose Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Medisense, Inc.
- Decided: Feb 26, 1990 after 73 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.
61 later devices descend from it; 1 cites it directly.
3 of 62 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
- 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
- K052980: Liberty Glucose Control, Model 2120031 (2005), 19 descendants of its own
- K040814: Modification to Precision Xtra Advanced Diabetes Management System (2004), 16 descendants of its own

Source page: https://510kreport.com/device/K896951
Methodology: https://510kreport.com/methodology