← Product Code [FFX](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/FFX) · K011472

# POLYGRAM 98 ANORECTAL FUNCTION TESTING APPLICATION, POLYGRAM 98 ESOPHAGEAL MANOMETRY APPLICATION, POLYGRAF ID (K011472)

_Medtronic Functional Diagnostics A/S · FFX · Aug 10, 2001 · Gastroenterology, Urology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/FFX/K011472

## Device Facts

- **Applicant:** Medtronic Functional Diagnostics A/S
- **Product Code:** [FFX](/submissions/GU/subpart-b%E2%80%94diagnostic-devices/FFX.md)
- **Decision Date:** Aug 10, 2001
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 876.1725
- **Device Class:** Class 2
- **Review Panel:** Gastroenterology, Urology

## Regulatory Identification

A gastrointestinal motility monitoring system is a device used to measure peristalic activity or pressure in the stomach or esophagus by means of a probe with transducers that is introduced through the mouth into the gastrointestinal tract. The device may include signal conditioning, amplifying, and recording equipment. This generic type of device includes the esophageal motility monitor and tube, the gastrointestinal motility (electrical) system, and certain accessories, such as a pressure transducer, amplifier, and external recorder.

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**Source:** [https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/FFX/K011472](https://fda.innolitics.com/submissions/GU/subpart-b%E2%80%94diagnostic-devices/FFX/K011472)

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