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FDA 510(k)

M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS

K-Number: K942129 · 1994-06-22

ApplicantMag, Inc.
Decision Date1994-06-22
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS is the device name listed in this FDA 510(k) record. The listed applicant is Mag, Inc.. It received FDA 510(k) clearance on 1994-06-22 under 510(k) number K942129. 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 M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS?

M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS is a medical device that received FDA 510(k) clearance on 1994-06-22. The listed applicant is Mag, Inc.. The 510(k) number is K942129.

When did M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS receive FDA 510(k) clearance?

M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS received FDA 510(k) clearance on 1994-06-22, under 510(k) number K942129.

Who is the listed applicant for M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS?

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

What is the FDA product code for M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS?

The FDA product code for M.A.G INC. ADULT TEMPERATURE MONITORING ANESTHESIA CIRCUITS is CAI.

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Other records listing Mag, 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.

K942132M.A.G. INC. HYPERINFLATION SYSTEMK942134M.A.G. INC. BREALTHING BAGSK942136M.A.G. INC PEDIATRIC TEMPERATURE MONITORING CIRCUITSK942135M.A.G. INC. COAXIAL CIRCUITSK942131M.A.G. INC. GUEDEL AIRWAYSK942127M.A.G INC. PEDIATRIC GAS SAMPLING CIRCUITS

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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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