ABL835 FLEX ANALYZER WITH PLEURAL PH
K-Number: K110416 · 2011-03-24
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Device Summary
Frequently Asked Questions
What is the ABL835 FLEX ANALYZER WITH PLEURAL PH?
ABL835 FLEX ANALYZER WITH PLEURAL PH is a medical device that received FDA 510(k) clearance on 2011-03-24. The listed applicant is Radiometer Medical Aps. The 510(k) number is K110416.
When did ABL835 FLEX ANALYZER WITH PLEURAL PH receive FDA 510(k) clearance?
ABL835 FLEX ANALYZER WITH PLEURAL PH received FDA 510(k) clearance on 2011-03-24, under 510(k) number K110416.
Who is the listed applicant for ABL835 FLEX ANALYZER WITH PLEURAL PH?
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 ABL835 FLEX ANALYZER WITH PLEURAL PH?
The FDA product code for ABL835 FLEX ANALYZER WITH PLEURAL PH 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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