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FDA 510(k)

EASYFLOW AIRWAY ADAPTER

K-Number: K935044 · 1993-11-18

ApplicantEasyflow Airway Systems, Inc.
Decision Date1993-11-18
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EASYFLOW AIRWAY ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Easyflow Airway Systems, Inc.. It received FDA 510(k) clearance on 1993-11-18 under 510(k) number K935044. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYFLOW AIRWAY ADAPTER?

EASYFLOW AIRWAY ADAPTER is a medical device that received FDA 510(k) clearance on 1993-11-18. The listed applicant is Easyflow Airway Systems, Inc.. The 510(k) number is K935044.

When did EASYFLOW AIRWAY ADAPTER receive FDA 510(k) clearance?

EASYFLOW AIRWAY ADAPTER received FDA 510(k) clearance on 1993-11-18, under 510(k) number K935044.

Who is the listed applicant for EASYFLOW AIRWAY ADAPTER?

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

What is the FDA product code for EASYFLOW AIRWAY ADAPTER?

The FDA product code for EASYFLOW AIRWAY ADAPTER is CAI.

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Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

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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