SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM)
K-Number: K897039 · 1990-03-16
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Device Summary
Frequently Asked Questions
What is the SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM)?
SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM) is a medical device that received FDA 510(k) clearance on 1990-03-16. The listed applicant is 3M Company. The 510(k) number is K897039.
When did SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM) receive FDA 510(k) clearance?
SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM) received FDA 510(k) clearance on 1990-03-16, under 510(k) number K897039.
Who is the listed applicant for SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM)?
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 MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM)?
The FDA product code for SARNS MINIPRIME CARDIOPLEGIA SET W/CONDUCER(TM) is DTR.
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: DTR)
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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