# K162412: Hoggan Scientific® microFET2™

- Pathway: 510(k) (Traditional)
- Applicant: Hoggan Scientific, LLC
- Decided: Mar 9, 2017 after 192 days
- Product code: LBB (Dynamometer, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 888.1240
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K042889 (2004). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042889: Dynamometer - Model Fce and Model MSC, Ametek (2004) Summary page 4.

## Indications for use
The microFET2™ System is a dynamometer device for performing muscle tests to quantitatively measure muscle weakness caused by injury or for sports medicine applications, as well as measure general muscle strength. The device is used to record and convey an individual's ability to resist force for a specific muscle or muscle group being tested.

Source page: https://510kreport.com/device/K162412
Methodology: https://510kreport.com/methodology