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FDA 510(k)

OXYGEN REGULATOR/FLOWMETER

K-Number: K780359 · 1978-04-04

ApplicantErie Mfg., Co.
Decision Date1978-04-04
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN REGULATOR/FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Erie Mfg., Co.. It received FDA 510(k) clearance on 1978-04-04 under 510(k) number K780359. 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 OXYGEN REGULATOR/FLOWMETER?

OXYGEN REGULATOR/FLOWMETER is a medical device that received FDA 510(k) clearance on 1978-04-04. The listed applicant is Erie Mfg., Co.. The 510(k) number is K780359.

When did OXYGEN REGULATOR/FLOWMETER receive FDA 510(k) clearance?

OXYGEN REGULATOR/FLOWMETER received FDA 510(k) clearance on 1978-04-04, under 510(k) number K780359.

Who is the listed applicant for OXYGEN REGULATOR/FLOWMETER?

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

What is the FDA product code for OXYGEN REGULATOR/FLOWMETER?

The FDA product code for OXYGEN REGULATOR/FLOWMETER 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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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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