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)

FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5

K-Number: K091723 · 2009-07-06

Decision Date2009-07-06
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5 is the device name listed in this FDA 510(k) record. The listed applicant is Freedom Sciences, LLC. It received FDA 510(k) clearance on 2009-07-06 under 510(k) number K091723. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5?

FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5 is a medical device that received FDA 510(k) clearance on 2009-07-06. The listed applicant is Freedom Sciences, LLC. The 510(k) number is K091723.

When did FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5 receive FDA 510(k) clearance?

FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5 received FDA 510(k) clearance on 2009-07-06, under 510(k) number K091723.

Who is the listed applicant for FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5?

The FDA 510(k) record lists Freedom Sciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5?

The FDA product code for FREEDOM SCIENCES MOTION CONTROL MODULE VERSION 1.5 is ITI.

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 Freedom Sciences, LLC 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: ITI)

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.

↑