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FDA 510(k)

VELOCITYAIS

K-Number: K070248 · 2007-03-01

ApplicantVelocity Medical Solutions, LLC
Decision Date2007-03-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VELOCITYAIS is the device name listed in this FDA 510(k) record. The listed applicant is Velocity Medical Solutions, LLC. It received FDA 510(k) clearance on 2007-03-01 under 510(k) number K070248. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VELOCITYAIS?

VELOCITYAIS is a medical device that received FDA 510(k) clearance on 2007-03-01. The listed applicant is Velocity Medical Solutions, LLC. The 510(k) number is K070248.

When did VELOCITYAIS receive FDA 510(k) clearance?

VELOCITYAIS received FDA 510(k) clearance on 2007-03-01, under 510(k) number K070248.

Who is the listed applicant for VELOCITYAIS?

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

What is the FDA product code for VELOCITYAIS?

The FDA product code for VELOCITYAIS is LLZ.

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.

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Other records listing Velocity Medical Solutions, 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.

K081076VELOCITYAIS, VELOCITY AI, VELOCITYVX, VELOCITYRT, V-RESPONSE

Related Devices (Code: LLZ)

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.

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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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