INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY
K-Number: K870911 · 1987-05-29
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Device Summary
Frequently Asked Questions
What is the INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY?
INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is American Bentley. The 510(k) number is K870911.
When did INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY receive FDA 510(k) clearance?
INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY received FDA 510(k) clearance on 1987-05-29, under 510(k) number K870911.
Who is the listed applicant for INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY?
The FDA 510(k) record lists American Bentley as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY?
The FDA product code for INDWELLING BLOOD CARBONDIOXIDE PARTIAL PRES. ANALY is CCC.
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 American Bentley 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: CCC)
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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