SIMPLICITY STARPLUS SOFT INFUSION SET
K-Number: K014061 · 2002-01-17
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Device Summary
Frequently Asked Questions
What is the SIMPLICITY STARPLUS SOFT INFUSION SET?
SIMPLICITY STARPLUS SOFT INFUSION SET is a medical device that received FDA 510(k) clearance on 2002-01-17. The listed applicant is Sterling Medivations, Inc.. The 510(k) number is K014061.
When did SIMPLICITY STARPLUS SOFT INFUSION SET receive FDA 510(k) clearance?
SIMPLICITY STARPLUS SOFT INFUSION SET received FDA 510(k) clearance on 2002-01-17, under 510(k) number K014061.
Who is the listed applicant for SIMPLICITY STARPLUS SOFT INFUSION SET?
The FDA 510(k) record lists Sterling Medivations, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SIMPLICITY STARPLUS SOFT INFUSION SET?
The FDA product code for SIMPLICITY STARPLUS SOFT INFUSION SET 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 Sterling Medivations, 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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