ACID BASE SYSTEM, RADIOMETER AUTOMATED
K-Number: K760229 · 1976-08-26
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Device Summary
Frequently Asked Questions
What is the ACID BASE SYSTEM, RADIOMETER AUTOMATED?
ACID BASE SYSTEM, RADIOMETER AUTOMATED is a medical device that received FDA 510(k) clearance on 1976-08-26. The listed applicant is The London Co.. The 510(k) number is K760229.
When did ACID BASE SYSTEM, RADIOMETER AUTOMATED receive FDA 510(k) clearance?
ACID BASE SYSTEM, RADIOMETER AUTOMATED received FDA 510(k) clearance on 1976-08-26, under 510(k) number K760229.
Who is the listed applicant for ACID BASE SYSTEM, RADIOMETER AUTOMATED?
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 ACID BASE SYSTEM, RADIOMETER AUTOMATED?
The FDA product code for ACID BASE SYSTEM, RADIOMETER AUTOMATED 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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