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FDA 510(k)

DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS

K-Number: K921624 · 1992-06-30

ApplicantIntertech Resources, Inc.
Decision Date1992-06-30
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1992-06-30 under 510(k) number K921624. 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 DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS?

DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS is a medical device that received FDA 510(k) clearance on 1992-06-30. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K921624.

When did DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS receive FDA 510(k) clearance?

DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS received FDA 510(k) clearance on 1992-06-30, under 510(k) number K921624.

Who is the listed applicant for DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS?

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

What is the FDA product code for DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS?

The FDA product code for DISPOSABLE VOLUME VENT/ANESTHESIA BREATH CIRCUITS is BYH.

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Other records listing Intertech Resources, 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952223XENON GAS BREATHING CIRCUITK952062PFT FILTERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC

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Related Devices (Code: BYH)

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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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