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FDA 510(k)

MAVEN PRO

K-Number: K130242 · 2013-08-29

ApplicantNsequence
Decision Date2013-08-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MAVEN PRO is the device name listed in this FDA 510(k) record. The listed applicant is Nsequence. It received FDA 510(k) clearance on 2013-08-29 under 510(k) number K130242. 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 MAVEN PRO?

MAVEN PRO is a medical device that received FDA 510(k) clearance on 2013-08-29. The listed applicant is Nsequence. The 510(k) number is K130242.

When did MAVEN PRO receive FDA 510(k) clearance?

MAVEN PRO received FDA 510(k) clearance on 2013-08-29, under 510(k) number K130242.

Who is the listed applicant for MAVEN PRO?

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

What is the FDA product code for MAVEN PRO?

The FDA product code for MAVEN PRO is LLZ.

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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

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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