Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MOTILITY VISUALIZATION SYSTEM

K-Number: K031169 · 2003-12-12

Decision Date2003-12-12
Product CodeFFX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOTILITY VISUALIZATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sierra Scientific Instruments, Inc.. It received FDA 510(k) clearance on 2003-12-12 under 510(k) number K031169. The device is classified under product code FFX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOTILITY VISUALIZATION SYSTEM?

MOTILITY VISUALIZATION SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-12. The listed applicant is Sierra Scientific Instruments, Inc.. The 510(k) number is K031169.

When did MOTILITY VISUALIZATION SYSTEM receive FDA 510(k) clearance?

MOTILITY VISUALIZATION SYSTEM received FDA 510(k) clearance on 2003-12-12, under 510(k) number K031169.

Who is the listed applicant for MOTILITY VISUALIZATION SYSTEM?

The FDA 510(k) record lists Sierra Scientific Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOTILITY VISUALIZATION SYSTEM?

The FDA product code for MOTILITY VISUALIZATION SYSTEM is FFX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Sierra Scientific Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FFX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑