FDA 510(k)

AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S

K-Number: K770001 · 1977-01-12

Decision Date1977-01-12

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S is the device name listed in this FDA 510(k) record. The listed applicant is Omnicon Medical Corp.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K770001. 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 AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S?

AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Omnicon Medical Corp.. The 510(k) number is K770001.

When did AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S receive FDA 510(k) clearance?

AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S received FDA 510(k) clearance on 1977-01-12, under 510(k) number K770001.

Who is the listed applicant for AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S?

The FDA 510(k) record lists Omnicon Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S?

The FDA product code for AIRWAY, BERMAN 40, 60, 80, 90, L00MM'S is CAE.

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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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.