FREEDOM 19 RECREATIONAL WHEELCHAIR
K-Number: K831510 · 1983-07-19
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Device Summary
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.
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