# K973914: Sense Technology Inc. Fras, Sense Technology Inc. Pulstar

- Pathway: 510(k) (Traditional)
- Applicant: Sense Technology, Inc.
- Decided: Jun 30, 1998 after 259 days
- Product code: LXM (Manipulator, Plunger-Like Joint)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K080261: Impulse IQ Adjusting Instrument (2008), 2 descendants of its own
- K160278: VSTAAR AdjusteR (2016), 0 descendants of its own
- K082218: Max Adjusting Instrument (2008), 0 descendants of its own

## Indications for use
Indications for use of the PulStarFRAS include: musculoskeletal pain due to joint subluxation, restricted joint mobility, myofacial spasm, ligamentous strain.

Source page: https://510kreport.com/device/K973914
Methodology: https://510kreport.com/methodology