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FDA 510(k)

HEATER, OXIMETER SYSTEM

K-Number: K781879 · 1979-01-08

Decision Date1979-01-08
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEATER, OXIMETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Oximetrix, Inc.. It received FDA 510(k) clearance on 1979-01-08 under 510(k) number K781879. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 12 devices →

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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