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FDA 510(k)

ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE

K-Number: K854573 · 1986-01-03

ApplicantArtec Environmental Monitoring Division
Decision Date1986-01-03
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE is the device name listed in this FDA 510(k) record. The listed applicant is Artec Environmental Monitoring Division. It received FDA 510(k) clearance on 1986-01-03 under 510(k) number K854573. 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 ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE?

ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE is a medical device that received FDA 510(k) clearance on 1986-01-03. The listed applicant is Artec Environmental Monitoring Division. The 510(k) number is K854573.

When did ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE receive FDA 510(k) clearance?

ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE received FDA 510(k) clearance on 1986-01-03, under 510(k) number K854573.

Who is the listed applicant for ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE?

The FDA 510(k) record lists Artec Environmental Monitoring Division as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE?

The FDA product code for ANESTHESIA SHUTOFF VALVE POSITIVE CLOSURE is CAI.

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Other records listing Artec Environmental Monitoring Division 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.

K900839THE CAROLINA ROCKERK896886ARTEC RESPOND PULMONARY RESUSCITATORK873043MOUTH TO FACE RESUSCITATORK863910RAINCOATK832512AIRWAY MASKSK830056ARTEC TWIST VALVE

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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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