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FDA 510(k)

GOODKNIGHT 425ST

K-Number: K050072 · 2005-06-13

ApplicantNellcor Puritan Bennett, Inc.
Decision Date2005-06-13
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GOODKNIGHT 425ST is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett, Inc.. It received FDA 510(k) clearance on 2005-06-13 under 510(k) number K050072. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GOODKNIGHT 425ST?

GOODKNIGHT 425ST is a medical device that received FDA 510(k) clearance on 2005-06-13. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K050072.

When did GOODKNIGHT 425ST receive FDA 510(k) clearance?

GOODKNIGHT 425ST received FDA 510(k) clearance on 2005-06-13, under 510(k) number K050072.

Who is the listed applicant for GOODKNIGHT 425ST?

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

What is the FDA product code for GOODKNIGHT 425ST?

The FDA product code for GOODKNIGHT 425ST is BZD.

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Other records listing Nellcor Puritan Bennett, Inc. as applicant

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Related Devices (Code: BZD)

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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