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FDA 510(k)

AIRCO NITROUS OXIDE REGULATOR

K-Number: K850106 · 1985-01-24

ApplicantAirco, Inc.
Decision Date1985-01-24
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRCO NITROUS OXIDE REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Airco, Inc.. It received FDA 510(k) clearance on 1985-01-24 under 510(k) number K850106. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRCO NITROUS OXIDE REGULATOR?

AIRCO NITROUS OXIDE REGULATOR is a medical device that received FDA 510(k) clearance on 1985-01-24. The listed applicant is Airco, Inc.. The 510(k) number is K850106.

When did AIRCO NITROUS OXIDE REGULATOR receive FDA 510(k) clearance?

AIRCO NITROUS OXIDE REGULATOR received FDA 510(k) clearance on 1985-01-24, under 510(k) number K850106.

Who is the listed applicant for AIRCO NITROUS OXIDE REGULATOR?

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

What is the FDA product code for AIRCO NITROUS OXIDE REGULATOR?

The FDA product code for AIRCO NITROUS OXIDE REGULATOR is CAN.

Related Clinical Trials

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.

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Other records listing Airco, 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.

K862796AIRCO PRESSURE REGULATORSK862797AIRCO 2000 SERIES FLOWMETERS

Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., 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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