Pump, infusion, implanted, programmable
PMA Number: P140032 · 2021-08-31
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Device Summary
Frequently Asked Questions
What is the Pump, infusion, implanted, programmable?
Pump, infusion, implanted, programmable is a medical device that received FDA 510(k) clearance on 2021-08-31. The listed applicant is Medtronic, Inc..
When did Pump, infusion, implanted, programmable receive FDA 510(k) clearance?
The clearance date for Pump, infusion, implanted, programmable can be found in the official FDA records.
Who is the listed applicant for Pump, infusion, implanted, programmable?
The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Pump, infusion, implanted, programmable?
The FDA product code for Pump, infusion, implanted, programmable is LKK.
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.
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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