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FDA 510(k)

CIRCUIT, BREATHING

K-Number: K811700 · 1981-07-10

ApplicantMarquest Medical Products, Inc.
Decision Date1981-07-10
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRCUIT, BREATHING 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 1981-07-10 under 510(k) number K811700. 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 CIRCUIT, BREATHING?

CIRCUIT, BREATHING is a medical device that received FDA 510(k) clearance on 1981-07-10. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K811700.

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

CIRCUIT, BREATHING received FDA 510(k) clearance on 1981-07-10, under 510(k) number K811700.

Who is the listed applicant for CIRCUIT, BREATHING?

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 CIRCUIT, BREATHING?

The FDA product code for CIRCUIT, BREATHING is CAI.

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Other records listing Marquest Medical Products, 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.

K050066C-CO2 COLORIMETRIC CO2 INDICATORK970478SCT 3000 HEATED HUMIDIFIERK962220HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIERK962223WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIERK960972DISPOSABLE GAS SAMPLING INTERFACE KITSK961838RESPIRGARD II, SPIROGARD

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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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