SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380
K-Number: K895632 · 1989-12-12
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Device Summary
Frequently Asked Questions
What is the SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380?
SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380 is a medical device that received FDA 510(k) clearance on 1989-12-12. The listed applicant is 3M Company. The 510(k) number is K895632.
When did SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380 receive FDA 510(k) clearance?
SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380 received FDA 510(k) clearance on 1989-12-12, under 510(k) number K895632.
Who is the listed applicant for SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380?
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 SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380?
The FDA product code for SARNS MEMBRANE OXYGENATOR W/INTEGRAL CADIO. 16380 is DTZ.
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: DTZ)
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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