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FDA 510(k)

AQUA TRAP

K-Number: K834573 · 1984-03-05

ApplicantAirlife, Inc.
Decision Date1984-03-05
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AQUA TRAP is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1984-03-05 under 510(k) number K834573. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUA TRAP?

AQUA TRAP is a medical device that received FDA 510(k) clearance on 1984-03-05. The listed applicant is Airlife, Inc.. The 510(k) number is K834573.

When did AQUA TRAP receive FDA 510(k) clearance?

AQUA TRAP received FDA 510(k) clearance on 1984-03-05, under 510(k) number K834573.

Who is the listed applicant for AQUA TRAP?

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

What is the FDA product code for AQUA TRAP?

The FDA product code for AQUA TRAP is BYH.

Other records listing Airlife, Inc. 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.

K834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASKK831246WHISTLER IN-LINE PRESSURE RELEASE VALVE

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Related Devices (Code: BYH)

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.

K946057AQUALARM MOISTURE SENSOR MODEL P85000Pegasus Research Corp.K932722CARIE MED-TECH MODEL 210 RAINOUT DRAINAGE SYSTEMCarie Med-Tech Services, Inc.K921624DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITSIntertech Resources, Inc.K900047THAYER SUCTION EVACUATION CONDENSATE COLLECTIONThayer Medical Corp.K897057THAYER SEMI-RIGID CONDENSATE COLLECTION SYSTEMThayer Medical Corp.K900591VENT-TRAP CAT# WR1000Ventlab Corp.

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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