HEATER, OXIMETER SYSTEM
K-Number: K781879 · 1979-01-08
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Device Summary
Frequently Asked Questions
What is the HEATER, OXIMETER SYSTEM?
HEATER, OXIMETER SYSTEM is a medical device that received FDA 510(k) clearance on 1979-01-08. The listed applicant is Oximetrix, Inc.. The 510(k) number is K781879.
When did HEATER, OXIMETER SYSTEM receive FDA 510(k) clearance?
HEATER, OXIMETER SYSTEM received FDA 510(k) clearance on 1979-01-08, under 510(k) number K781879.
Who is the listed applicant for HEATER, OXIMETER SYSTEM?
The FDA 510(k) record lists Oximetrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEATER, OXIMETER SYSTEM?
The FDA product code for HEATER, OXIMETER SYSTEM is DQA.
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 Oximetrix, 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: DQA)
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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