O2N DEMAND-II, VICTOR MODEL OCPR-II
K-Number: K992659 · 1999-09-03
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Device Summary
Frequently Asked Questions
What is the O2N DEMAND-II, VICTOR MODEL OCPR-II?
O2N DEMAND-II, VICTOR MODEL OCPR-II is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Thermadyne Holings Corp.. The 510(k) number is K992659.
When did O2N DEMAND-II, VICTOR MODEL OCPR-II receive FDA 510(k) clearance?
O2N DEMAND-II, VICTOR MODEL OCPR-II received FDA 510(k) clearance on 1999-09-03, under 510(k) number K992659.
Who is the listed applicant for O2N DEMAND-II, VICTOR MODEL OCPR-II?
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 O2N DEMAND-II, VICTOR MODEL OCPR-II?
The FDA product code for O2N DEMAND-II, VICTOR MODEL OCPR-II is NFB.
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: NFB)
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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