CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED
K-Number: K912030 · 1991-10-30
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Device Summary
Frequently Asked Questions
What is the CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED?
CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED is a medical device that received FDA 510(k) clearance on 1991-10-30. The listed applicant is 3M Company. The 510(k) number is K912030.
When did CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED receive FDA 510(k) clearance?
CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED received FDA 510(k) clearance on 1991-10-30, under 510(k) number K912030.
Who is the listed applicant for CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED?
The FDA product code for CDI(TM) 2000 BLOOD GAS MONITORING SYST, MODIFIED is CBZ.
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 3M Company 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: CBZ)
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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