ABL90 FLEX
K-Number: K123748 · 2013-05-07
Advertisement
Device Summary
Frequently Asked Questions
What is the ABL90 FLEX?
ABL90 FLEX is a medical device that received FDA 510(k) clearance on 2013-05-07. The listed applicant is Radiometer Medical Aps. The 510(k) number is K123748.
When did ABL90 FLEX receive FDA 510(k) clearance?
ABL90 FLEX received FDA 510(k) clearance on 2013-05-07, under 510(k) number K123748.
Who is the listed applicant for ABL90 FLEX?
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?
The FDA product code for ABL90 FLEX is CHL.
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.
Advertisement