SIMPLICITY SOFT QD SILVER INFUSION SET
K-Number: K011580 · 2001-06-05
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Device Summary
Frequently Asked Questions
What is the SIMPLICITY SOFT QD SILVER INFUSION SET?
SIMPLICITY SOFT QD SILVER INFUSION SET is a medical device that received FDA 510(k) clearance on 2001-06-05. The listed applicant is Sterling Medivations, Inc.. The 510(k) number is K011580.
When did SIMPLICITY SOFT QD SILVER INFUSION SET receive FDA 510(k) clearance?
SIMPLICITY SOFT QD SILVER INFUSION SET received FDA 510(k) clearance on 2001-06-05, under 510(k) number K011580.
Who is the listed applicant for SIMPLICITY SOFT QD SILVER 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 SOFT QD SILVER INFUSION SET?
The FDA product code for SIMPLICITY SOFT QD SILVER 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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