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FDA 510(k)

NUMALINK

K-Number: K002724 · 2000-11-17

ApplicantNuma, Inc.
Decision Date2000-11-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NUMALINK is the device name listed in this FDA 510(k) record. The listed applicant is Numa, Inc.. It received FDA 510(k) clearance on 2000-11-17 under 510(k) number K002724. 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 NUMALINK?

NUMALINK is a medical device that received FDA 510(k) clearance on 2000-11-17. The listed applicant is Numa, Inc.. The 510(k) number is K002724.

When did NUMALINK receive FDA 510(k) clearance?

NUMALINK received FDA 510(k) clearance on 2000-11-17, under 510(k) number K002724.

Who is the listed applicant for NUMALINK?

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

What is the FDA product code for NUMALINK?

The FDA product code for NUMALINK is LLZ.

Related Clinical Trials

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Other records listing Numa, Inc. 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.

K974444NUMASTATION

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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