PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325
K-Number: K001827 · 2000-08-18
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Device Summary
Frequently Asked Questions
What is the PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325?
PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325 is a medical device that received FDA 510(k) clearance on 2000-08-18. The listed applicant is Minimed, Inc.. The 510(k) number is K001827.
When did PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325 receive FDA 510(k) clearance?
PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325 received FDA 510(k) clearance on 2000-08-18, under 510(k) number K001827.
Who is the listed applicant for PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325?
The FDA 510(k) record lists Minimed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325?
The FDA product code for PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325 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 Minimed, Inc. 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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