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FDA 510(k)

KOKO LEGEND

K-Number: K051572 · 2005-11-17

ApplicantPulmonary Data Services, Inc.
Decision Date2005-11-17
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

KOKO LEGEND is the device name listed in this FDA 510(k) record. The listed applicant is Pulmonary Data Services, Inc.. It received FDA 510(k) clearance on 2005-11-17 under 510(k) number K051572. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOKO LEGEND?

KOKO LEGEND is a medical device that received FDA 510(k) clearance on 2005-11-17. The listed applicant is Pulmonary Data Services, Inc.. The 510(k) number is K051572.

When did KOKO LEGEND receive FDA 510(k) clearance?

KOKO LEGEND received FDA 510(k) clearance on 2005-11-17, under 510(k) number K051572.

Who is the listed applicant for KOKO LEGEND?

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

What is the FDA product code for KOKO LEGEND?

The FDA product code for KOKO LEGEND is BZG.

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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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