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FDA 510(k)

FREEDOM

K-Number: K823849 · 1983-04-12

Decision Date1983-04-12
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FREEDOM is the device name listed in this FDA 510(k) record. The listed applicant is Carbonite Corp.. It received FDA 510(k) clearance on 1983-04-12 under 510(k) number K823849. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEDOM?

FREEDOM is a medical device that received FDA 510(k) clearance on 1983-04-12. The listed applicant is Carbonite Corp.. The 510(k) number is K823849.

When did FREEDOM receive FDA 510(k) clearance?

FREEDOM received FDA 510(k) clearance on 1983-04-12, under 510(k) number K823849.

Who is the listed applicant for FREEDOM?

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?

The FDA product code for FREEDOM is IOR.

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: IOR)

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

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

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