FDA 510(k)

VENTILATOR BREATHING CIRCUIT

K-Number: K770286 · 1977-02-25

Decision Date1977-02-25

Product CodeCAI

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

VENTILATOR BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Mcgaw Respiratory Therapy. It received FDA 510(k) clearance on 1977-02-25 under 510(k) number K770286. 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 VENTILATOR BREATHING CIRCUIT?

VENTILATOR BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1977-02-25. The listed applicant is Mcgaw Respiratory Therapy. The 510(k) number is K770286.

When did VENTILATOR BREATHING CIRCUIT receive FDA 510(k) clearance?

VENTILATOR BREATHING CIRCUIT received FDA 510(k) clearance on 1977-02-25, under 510(k) number K770286.

Who is the listed applicant for VENTILATOR BREATHING CIRCUIT?

The FDA 510(k) record lists Mcgaw Respiratory Therapy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTILATOR BREATHING CIRCUIT?

The FDA product code for VENTILATOR BREATHING CIRCUIT is CAI.

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Other records listing Mcgaw Respiratory Therapy as applicant

K771550MRT DISPENSOR K771516CAPILLARY SAMPLE LINE K770665VALVE, PRESSURE, DEMAND K761299DISPOSABLE NEBULIZER K761300NEBULIZER CONTROL UNIT K761298PRE-FILLED DISPOSABLE NEBULIZER

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Related Devices (Code: CAI)

K954480CONDENSATE COLLECTION KITNova-Ventrx K953787UNICOR, 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.