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FDA 510(k)

PRECISION GAS MIXER

K-Number: K781417 · 1978-09-20

ApplicantMedicor USA , Ltd.
Decision Date1978-09-20
Product CodeLCH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRECISION GAS MIXER is the device name listed in this FDA 510(k) record. The listed applicant is Medicor USA , Ltd.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781417. The device is classified under product code LCH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRECISION GAS MIXER?

PRECISION GAS MIXER is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Medicor USA , Ltd.. The 510(k) number is K781417.

When did PRECISION GAS MIXER receive FDA 510(k) clearance?

PRECISION GAS MIXER received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781417.

Who is the listed applicant for PRECISION GAS MIXER?

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

What is the FDA product code for PRECISION GAS MIXER?

The FDA product code for PRECISION GAS MIXER is LCH.

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Other records listing Medicor USA , Ltd. as applicant

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Related Devices (Code: LCH)

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.

K922386RNA MEDICAL TONOMETERBionostics, Inc.K904163CLINICAL BLOOD GAS MIXTURESNorco, Inc.K900819BLOOD GAS CALIBRATION STANDARDCryogenic Rare Gas Laboratories, Inc.K862958AMR RESEARCH TONOMETERAssociated Medical RepresentativesK841089LINEAR CLOUD TONOMETERLinear Tonometers, Inc.K802379HEM-O-SCAN OXYGEN EQUIL. CURVE ANALYZERAmerican Instrument Co.

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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