INTRAVASCULAR ADMINISTRATION SET MODEL 60040
K-Number: K891009 · 1989-05-16
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Device Summary
Frequently Asked Questions
What is the INTRAVASCULAR ADMINISTRATION SET MODEL 60040?
INTRAVASCULAR ADMINISTRATION SET MODEL 60040 is a medical device that received FDA 510(k) clearance on 1989-05-16. The listed applicant is 3M Company. The 510(k) number is K891009.
When did INTRAVASCULAR ADMINISTRATION SET MODEL 60040 receive FDA 510(k) clearance?
INTRAVASCULAR ADMINISTRATION SET MODEL 60040 received FDA 510(k) clearance on 1989-05-16, under 510(k) number K891009.
Who is the listed applicant for INTRAVASCULAR ADMINISTRATION SET MODEL 60040?
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 INTRAVASCULAR ADMINISTRATION SET MODEL 60040?
The FDA product code for INTRAVASCULAR ADMINISTRATION SET MODEL 60040 is FPK.
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: FPK)
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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