# K033646: Trifit 700

- Pathway: 510(k) (Traditional)
- Applicant: Healthfirst Corp.
- Decided: Mar 1, 2005 after 467 days
- Product code: DRT (Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- 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.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Microfit Fitness Evaluation System: named in the summary without a submission number

## Indications for use
The TriFIT 700M is a physical fitness assessment device which can be used in both medical and non-medical settings. It is used for individuals to test and to measure their physical fitness levels. The assessment includes body weight, biceps strength, flexibility, skin-fold thickness (to estimate percentage body fat), and heart rate.

Source page: https://510kreport.com/device/K033646
Methodology: https://510kreport.com/methodology