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FDA 510(k)

BROOK LIFE SAVING AIRWAY DEVICE #900 &

K-Number: K832435 · 1983-10-04

ApplicantLa Societe Fianciere Senefin
Decision Date1983-10-04
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BROOK LIFE SAVING AIRWAY DEVICE #900 & is the device name listed in this FDA 510(k) record. The listed applicant is La Societe Fianciere Senefin. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832435. The device is classified under product code CAE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BROOK LIFE SAVING AIRWAY DEVICE #900 &?

BROOK LIFE SAVING AIRWAY DEVICE #900 & is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is La Societe Fianciere Senefin. The 510(k) number is K832435.

When did BROOK LIFE SAVING AIRWAY DEVICE #900 & receive FDA 510(k) clearance?

BROOK LIFE SAVING AIRWAY DEVICE #900 & received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832435.

Who is the listed applicant for BROOK LIFE SAVING AIRWAY DEVICE #900 &?

The FDA 510(k) record lists La Societe Fianciere Senefin as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BROOK LIFE SAVING AIRWAY DEVICE #900 &?

The FDA product code for BROOK LIFE SAVING AIRWAY DEVICE #900 & is CAE.

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Related Devices (Code: CAE)

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.

K033189KING LTS REUSABLE OROPHARYNGEAL AIRWAY WITH DRAIN/SUCTION CHANNEL, MODELS KLT 303, KLT 304 AND KLT 305King Systems Corp.K033186KING LT-D DISPOSABLE OROPHARYNGEAL AIRWAY, MODELS KLT 203, KLT 204 AND KLT 205King Systems Corp.K021634KING LT, MODELS # KLT 100, KLT 101, KLT 102, KLT 103, KLT 104, KLT 105King Systems Corp.K955721CUFFED OROPHARYNGEAL AIRWAY (COPA)Mallinckrodt MedicalK960240RUSCH OPTOSAFERusch Intl.K950613KEISEIKeisei (Usa) 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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