FDA 510(k)

ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III

K-Number: K832471 · 1983-09-12

Decision Date1983-09-12

Product CodeCAE

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832471. 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 ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III?

ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Inmed Corp.. The 510(k) number is K832471.

When did ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III receive FDA 510(k) clearance?

ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832471.

Who is the listed applicant for ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III?

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

What is the FDA product code for ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III?

The FDA product code for ADJUSTABLE PHARYNGEAL AIRWAY/BERMAN III is CAE.

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Other records listing Inmed Corp. as applicant

K862672ESOPHAGEAL STETHOSCOPE WITH THERMISTOR K853162STERILE NASOPHARYNGEAL AIRWAY K850335URETEROSCOPY CATHETER K850152PRECONNECTED URETHRAL CATHETER TRAY K850248DISPOSABLE GUEDEL AIRWAY K844801ULTRA EXTERNAL CATHETER

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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.