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FDA 510(k)

DISPOSABLE NON-REBREATHING ANES. CIRCUIT

K-Number: K823714 · 1983-01-07

ApplicantMarquest Medical Products, Inc.
Decision Date1983-01-07
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NON-REBREATHING ANES. CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1983-01-07 under 510(k) number K823714. 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 NON-REBREATHING ANES. CIRCUIT?

DISPOSABLE NON-REBREATHING ANES. CIRCUIT is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K823714.

When did DISPOSABLE NON-REBREATHING ANES. CIRCUIT receive FDA 510(k) clearance?

DISPOSABLE NON-REBREATHING ANES. CIRCUIT received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823714.

Who is the listed applicant for DISPOSABLE NON-REBREATHING ANES. CIRCUIT?

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

What is the FDA product code for DISPOSABLE NON-REBREATHING ANES. CIRCUIT?

The FDA product code for DISPOSABLE NON-REBREATHING ANES. CIRCUIT is CAI.

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Other records listing Marquest Medical Products, Inc. as applicant

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K050066C-CO2 COLORIMETRIC CO2 INDICATORK970478SCT 3000 HEATED HUMIDIFIERK962223WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIERK962220HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIERK961838RESPIRGARD II, SPIROGARDK960972DISPOSABLE GAS SAMPLING INTERFACE KITS

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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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