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FDA 510(k)

DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED

K-Number: K912504 · 1991-10-23

ApplicantIntertech Resources, Inc.
Decision Date1991-10-23
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED 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 1991-10-23 under 510(k) number K912504. 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 DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED?

DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED is a medical device that received FDA 510(k) clearance on 1991-10-23. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K912504.

When did DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED receive FDA 510(k) clearance?

DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED received FDA 510(k) clearance on 1991-10-23, under 510(k) number K912504.

Who is the listed applicant for DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED?

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 ANESTHESIA BREATHING CIRCUITS, MODIFIED?

The FDA product code for DISPOSABLE ANESTHESIA BREATHING CIRCUITS, MODIFIED is CAI.

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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 FILTERK952214SIMS INTERTECH HYPERINFLATION BAG SYSTEM

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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.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL 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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