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FDA 510(k)

VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED

K-Number: K891771 · 1989-06-23

Decision Date1989-06-23
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Thermadyne Holings Corp.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K891771. 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 VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED?

VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Thermadyne Holings Corp.. The 510(k) number is K891771.

When did VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED receive FDA 510(k) clearance?

VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED received FDA 510(k) clearance on 1989-06-23, under 510(k) number K891771.

Who is the listed applicant for VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED?

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

What is the FDA product code for VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED?

The FDA product code for VICTOR MEDICAL OXYGEN THERAPY REGULATOR, MODIFIED 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.

Other records listing Thermadyne Holings 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.

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.

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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