POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133
K-Number: K961474 · 1996-05-06
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Device Summary
Frequently Asked Questions
What is the POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133?
POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133 is a medical device that received FDA 510(k) clearance on 1996-05-06. The listed applicant is Medtronic Minimed. The 510(k) number is K961474.
When did POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133 receive FDA 510(k) clearance?
POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133 received FDA 510(k) clearance on 1996-05-06, under 510(k) number K961474.
Who is the listed applicant for POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133?
The FDA 510(k) record lists Medtronic Minimed as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133?
The FDA product code for POLYFIN INFUSION SET MMT-106/MMT-107/MMT-133 is FPA.
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 Medtronic Minimed 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: FPA)
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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