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FDA 510(k)

NELLCOR PURITAN BENNETT, GOODKNIGHT 418G

K-Number: K991150 · 1999-04-14

ApplicantNellcor Puritan Bennett France Dvpt.
Decision Date1999-04-14
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NELLCOR PURITAN BENNETT, GOODKNIGHT 418G is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett France Dvpt.. It received FDA 510(k) clearance on 1999-04-14 under 510(k) number K991150. 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 NELLCOR PURITAN BENNETT, GOODKNIGHT 418G?

NELLCOR PURITAN BENNETT, GOODKNIGHT 418G is a medical device that received FDA 510(k) clearance on 1999-04-14. The listed applicant is Nellcor Puritan Bennett France Dvpt.. The 510(k) number is K991150.

When did NELLCOR PURITAN BENNETT, GOODKNIGHT 418G receive FDA 510(k) clearance?

NELLCOR PURITAN BENNETT, GOODKNIGHT 418G received FDA 510(k) clearance on 1999-04-14, under 510(k) number K991150.

Who is the listed applicant for NELLCOR PURITAN BENNETT, GOODKNIGHT 418G?

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

What is the FDA product code for NELLCOR PURITAN BENNETT, GOODKNIGHT 418G?

The FDA product code for NELLCOR PURITAN BENNETT, GOODKNIGHT 418G is BZD.

Related Clinical Trials

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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Other records listing Nellcor Puritan Bennett France Dvpt. 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.

K993584MALLINCKRODT, GOODKNIGHT 418A, GOODKNIGHT 418P, SILVERLINING 2

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.

K261262Altis Full Face MaskRespironics, Inc.K253044RXiBreeze PAP System (RXiBreeze 20C)Resvent Medical Technology Co., Ltd.K253553OrionResmed CorpK254104ResScan EssentialsResmed CorpK251920Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face MaskDcstar, Inc.K253166F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical Co., Ltd.

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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