FDA 510(k)

#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY

K-Number: K883593 · 1988-09-30

Decision Date1988-09-30

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Ecolab, Inc.. It received FDA 510(k) clearance on 1988-09-30 under 510(k) number K883593. 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 #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY?

#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Ecolab, Inc.. The 510(k) number is K883593.

When did #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY receive FDA 510(k) clearance?

#400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883593.

Who is the listed applicant for #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY?

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

What is the FDA product code for #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY?

The FDA product code for #400 BROOK AIRWAY & #900 PROFESSIONAL BROOK AIRWAY is CAE.

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Other records listing Ecolab, Inc. as applicant

K182164Ecolab POU Water Filter Spray Outlet, Ecolab POU Water Filter Nozzle Outlet, Ecolab POU Water Filter Shower Wand K173164Ecolab POU Water Filter K152522ORS-3000LD Slush Drapes, ORS-1000LD Fluid Warming Drapes

Related Devices (Code: CAE)

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 Medical K960240RUSCH OPTOSAFERusch Intl.K950613KEISEIKeisei (Usa) Co., Ltd.

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.