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FDA 510(k)

RIND AIRWAY

K-Number: K812822 · 1981-11-16

ApplicantRind Medical Development
Decision Date1981-11-16
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RIND AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Rind Medical Development. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K812822. 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 RIND AIRWAY?

RIND AIRWAY is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is Rind Medical Development. The 510(k) number is K812822.

When did RIND AIRWAY receive FDA 510(k) clearance?

RIND AIRWAY received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812822.

Who is the listed applicant for RIND AIRWAY?

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

What is the FDA product code for RIND AIRWAY?

The FDA product code for RIND AIRWAY 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

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

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