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FDA 510(k)

INSPIRON LIQUID OXYGEN SYSTEM

K-Number: K834290 · 1984-02-04

Decision Date1984-02-04
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRON LIQUID OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1984-02-04 under 510(k) number K834290. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSPIRON LIQUID OXYGEN SYSTEM?

INSPIRON LIQUID OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 1984-02-04. The listed applicant is Inspiron Corp.. The 510(k) number is K834290.

When did INSPIRON LIQUID OXYGEN SYSTEM receive FDA 510(k) clearance?

INSPIRON LIQUID OXYGEN SYSTEM received FDA 510(k) clearance on 1984-02-04, under 510(k) number K834290.

Who is the listed applicant for INSPIRON LIQUID OXYGEN SYSTEM?

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

What is the FDA product code for INSPIRON LIQUID OXYGEN SYSTEM?

The FDA product code for INSPIRON LIQUID OXYGEN SYSTEM is BYJ.

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.

Other records listing Inspiron Corp. 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.

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Related Devices (Code: BYJ)

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.

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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