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FDA 510(k)

VOLUME VENTILATOR CIRCUIT W/WATER TRAP

K-Number: K834570 · 1984-03-05

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

Device Summary

VOLUME VENTILATOR CIRCUIT W/WATER 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 K834570. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLUME VENTILATOR CIRCUIT W/WATER TRAP?

VOLUME VENTILATOR CIRCUIT W/WATER 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 K834570.

When did VOLUME VENTILATOR CIRCUIT W/WATER TRAP receive FDA 510(k) clearance?

VOLUME VENTILATOR CIRCUIT W/WATER TRAP received FDA 510(k) clearance on 1984-03-05, under 510(k) number K834570.

Who is the listed applicant for VOLUME VENTILATOR CIRCUIT W/WATER 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 VOLUME VENTILATOR CIRCUIT W/WATER TRAP?

The FDA product code for VOLUME VENTILATOR CIRCUIT W/WATER TRAP is BZO.

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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.

K834573AQUA TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASKK831246WHISTLER IN-LINE PRESSURE RELEASE VALVE

View all 76 devices →

Related Devices (Code: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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