MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM
K-Number: K874663 · 1988-05-31
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Device Summary
Frequently Asked Questions
What is the MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM?
MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM is a medical device that received FDA 510(k) clearance on 1988-05-31. The listed applicant is Ametek/Thermox Instruments Division. The 510(k) number is K874663.
When did MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM receive FDA 510(k) clearance?
MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM received FDA 510(k) clearance on 1988-05-31, under 510(k) number K874663.
Who is the listed applicant for MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM?
The FDA 510(k) record lists Ametek/Thermox Instruments Division as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM?
The FDA product code for MOXUS OR OCM-1 OXYGEN UPTAKE SYSTEM is BZL.
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 Ametek/Thermox Instruments Division 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: BZL)
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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