INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050
K-Number: K891005 · 1989-05-11
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Device Summary
Frequently Asked Questions
What is the INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050?
INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050 is a medical device that received FDA 510(k) clearance on 1989-05-11. The listed applicant is 3M Company. The 510(k) number is K891005.
When did INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050 receive FDA 510(k) clearance?
INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050 received FDA 510(k) clearance on 1989-05-11, under 510(k) number K891005.
Who is the listed applicant for INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050?
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 ADMINI. SET MODELS 60030 & 60050?
The FDA product code for INTRAVASCULAR ADMINI. SET MODELS 60030 & 60050 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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