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FDA 510(k)

JIVE X SOFTWARE

K-Number: K053183 · 2006-02-16

ApplicantVisus Technology Transfer GmbH
Decision Date2006-02-16
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JIVE X SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Visus Technology Transfer GmbH. It received FDA 510(k) clearance on 2006-02-16 under 510(k) number K053183. 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 JIVE X SOFTWARE?

JIVE X SOFTWARE is a medical device that received FDA 510(k) clearance on 2006-02-16. The listed applicant is Visus Technology Transfer GmbH. The 510(k) number is K053183.

When did JIVE X SOFTWARE receive FDA 510(k) clearance?

JIVE X SOFTWARE received FDA 510(k) clearance on 2006-02-16, under 510(k) number K053183.

Who is the listed applicant for JIVE X SOFTWARE?

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

What is the FDA product code for JIVE X SOFTWARE?

The FDA product code for JIVE X SOFTWARE is LLZ.

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Other records listing Visus Technology Transfer GmbH 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.

K162008JiveX

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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