RADIOMETER ACID BASE LABORATORY-ABL-3
K-Number: K800224 · 1980-02-22
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Device Summary
Frequently Asked Questions
What is the RADIOMETER ACID BASE LABORATORY-ABL-3?
RADIOMETER ACID BASE LABORATORY-ABL-3 is a medical device that received FDA 510(k) clearance on 1980-02-22. The listed applicant is The London Co.. The 510(k) number is K800224.
When did RADIOMETER ACID BASE LABORATORY-ABL-3 receive FDA 510(k) clearance?
RADIOMETER ACID BASE LABORATORY-ABL-3 received FDA 510(k) clearance on 1980-02-22, under 510(k) number K800224.
Who is the listed applicant for RADIOMETER ACID BASE LABORATORY-ABL-3?
The FDA 510(k) record lists The London Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADIOMETER ACID BASE LABORATORY-ABL-3?
The FDA product code for RADIOMETER ACID BASE LABORATORY-ABL-3 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 The London Co. 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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