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 19 RECREATIONAL WHEELCHAIR

K-Number: K831510 · 1983-07-19

Decision Date1983-07-19
Product CodeIQC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FREEDOM 19 RECREATIONAL WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Carbonite Corp.. It received FDA 510(k) clearance on 1983-07-19 under 510(k) number K831510. The device is classified under product code IQC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM 19 RECREATIONAL WHEELCHAIR?

FREEDOM 19 RECREATIONAL WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is Carbonite Corp.. The 510(k) number is K831510.

When did FREEDOM 19 RECREATIONAL WHEELCHAIR receive FDA 510(k) clearance?

FREEDOM 19 RECREATIONAL WHEELCHAIR received FDA 510(k) clearance on 1983-07-19, under 510(k) number K831510.

Who is the listed applicant for FREEDOM 19 RECREATIONAL WHEELCHAIR?

The FDA 510(k) record lists Carbonite Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FREEDOM 19 RECREATIONAL WHEELCHAIR?

The FDA product code for FREEDOM 19 RECREATIONAL WHEELCHAIR is IQC.

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 Carbonite Corp. 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: IQC)

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.

↑