TIMOX OXYGEN TIMER
K-Number: K920360 · 1992-08-03
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Device Summary
Frequently Asked Questions
What is the TIMOX OXYGEN TIMER?
TIMOX OXYGEN TIMER is a medical device that received FDA 510(k) clearance on 1992-08-03. The listed applicant is Medical Fittings, Inc.. The 510(k) number is K920360.
When did TIMOX OXYGEN TIMER receive FDA 510(k) clearance?
TIMOX OXYGEN TIMER received FDA 510(k) clearance on 1992-08-03, under 510(k) number K920360.
Who is the listed applicant for TIMOX OXYGEN TIMER?
The FDA 510(k) record lists Medical Fittings, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TIMOX OXYGEN TIMER?
The FDA product code for TIMOX OXYGEN TIMER is BXP.
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 Medical Fittings, Inc. 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: BXP)
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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