ABL90 FLEX ANALYZER
K-Number: K131988 · 2013-09-17
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Device Summary
Frequently Asked Questions
What is the ABL90 FLEX ANALYZER?
ABL90 FLEX ANALYZER is a medical device that received FDA 510(k) clearance on 2013-09-17. The listed applicant is Radiometer Medical Aps. The 510(k) number is K131988.
When did ABL90 FLEX ANALYZER receive FDA 510(k) clearance?
ABL90 FLEX ANALYZER received FDA 510(k) clearance on 2013-09-17, under 510(k) number K131988.
Who is the listed applicant for ABL90 FLEX ANALYZER?
The FDA 510(k) record lists Radiometer Medical Aps as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABL90 FLEX ANALYZER?
The FDA product code for ABL90 FLEX ANALYZER is CHL.
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 Radiometer Medical Aps 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: CHL)
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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