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FDA 510(k)

DISPOSABLE BERMAN AND GUEDEL AIRWAYS

K-Number: K861540 · 1986-05-02

ApplicantDryden Corp.
Decision Date1986-05-02
Product CodeCAE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BERMAN AND GUEDEL AIRWAYS is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861540. 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 DISPOSABLE BERMAN AND GUEDEL AIRWAYS?

DISPOSABLE BERMAN AND GUEDEL AIRWAYS is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Dryden Corp.. The 510(k) number is K861540.

When did DISPOSABLE BERMAN AND GUEDEL AIRWAYS receive FDA 510(k) clearance?

DISPOSABLE BERMAN AND GUEDEL AIRWAYS received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861540.

Who is the listed applicant for DISPOSABLE BERMAN AND GUEDEL AIRWAYS?

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

What is the FDA product code for DISPOSABLE BERMAN AND GUEDEL AIRWAYS?

The FDA product code for DISPOSABLE BERMAN AND GUEDEL AIRWAYS is CAE.

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Other records listing Dryden Corp. as applicant

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.

K880923PATIENT VENTILATOR ISOLATORK880769BREATHING CIRCUIT W/HEATED WIREK882285NONREBREATHING CIRCUITK873928UNIVERSAL TOURNIQUETK873927REUSEABLE BREATHING TUBESK870859BAG-TAIL BLEED VALVE

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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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