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FDA 510(k)

AIRCO PRESSURE REGULATORS

K-Number: K862796 · 1986-08-08

ApplicantAirco, Inc.
Decision Date1986-08-08
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRCO PRESSURE REGULATORS is the device name listed in this FDA 510(k) record. The listed applicant is Airco, Inc.. It received FDA 510(k) clearance on 1986-08-08 under 510(k) number K862796. 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 PRESSURE REGULATORS?

AIRCO PRESSURE REGULATORS is a medical device that received FDA 510(k) clearance on 1986-08-08. The listed applicant is Airco, Inc.. The 510(k) number is K862796.

When did AIRCO PRESSURE REGULATORS receive FDA 510(k) clearance?

AIRCO PRESSURE REGULATORS received FDA 510(k) clearance on 1986-08-08, under 510(k) number K862796.

Who is the listed applicant for AIRCO PRESSURE REGULATORS?

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 PRESSURE REGULATORS?

The FDA product code for AIRCO PRESSURE REGULATORS 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.

K862797AIRCO 2000 SERIES FLOWMETERSK850106AIRCO NITROUS OXIDE REGULATOR

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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