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FDA 510(k)

CONI

K-Number: K130624 · 2013-05-07

ApplicantGlobalmed
Decision Date2013-05-07
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CONI is the device name listed in this FDA 510(k) record. The listed applicant is Globalmed. It received FDA 510(k) clearance on 2013-05-07 under 510(k) number K130624. 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 CONI?

CONI is a medical device that received FDA 510(k) clearance on 2013-05-07. The listed applicant is Globalmed. The 510(k) number is K130624.

When did CONI receive FDA 510(k) clearance?

CONI received FDA 510(k) clearance on 2013-05-07, under 510(k) number K130624.

Who is the listed applicant for CONI?

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

What is the FDA product code for CONI?

The FDA product code for CONI is LLZ.

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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