NIPRO INSULIN SYRINGE
K-Number: K000144 · 2000-02-11
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Device Summary
Frequently Asked Questions
What is the NIPRO INSULIN SYRINGE?
NIPRO INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 2000-02-11. The listed applicant is Nipro Medical Corp.. The 510(k) number is K000144.
When did NIPRO INSULIN SYRINGE receive FDA 510(k) clearance?
NIPRO INSULIN SYRINGE received FDA 510(k) clearance on 2000-02-11, under 510(k) number K000144.
Who is the listed applicant for NIPRO INSULIN SYRINGE?
The FDA 510(k) record lists Nipro Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIPRO INSULIN SYRINGE?
The FDA product code for NIPRO INSULIN SYRINGE is FMF.
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 Nipro Medical Corp. 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: FMF)
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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