MRL OXIMETER
K-Number: K882664 · 1988-09-16
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Device Summary
Frequently Asked Questions
What is the MRL OXIMETER?
MRL OXIMETER is a medical device that received FDA 510(k) clearance on 1988-09-16. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K882664.
When did MRL OXIMETER receive FDA 510(k) clearance?
MRL OXIMETER received FDA 510(k) clearance on 1988-09-16, under 510(k) number K882664.
Who is the listed applicant for MRL OXIMETER?
The FDA 510(k) record lists Medical Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MRL OXIMETER?
The FDA product code for MRL OXIMETER 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 Medical Research Laboratories, 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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