# K113074: Cmap Pro

- Pathway: 510(k) (Traditional)
- Applicant: Medical Technologies, Inc.
- Decided: Feb 2, 2012 after 108 days
- Product code: IKN (Electromyograph, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 890.1375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K890495 (1989). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031995: Comprehensive Neuromuscular Profiler, Medical Technologies Unlimited, Inc. (2004) Summary page 1.

## Most influential descendants
- K173510: BioStamp nPoint (2018), 0 descendants of its own

## Indications for use
Surface electromyography with video recording, range of motion tracking, isometric functional testing and pinch and grip strength measuring.

Source page: https://510kreport.com/device/K113074
Methodology: https://510kreport.com/methodology