NIPRO DISPOSABLE SYRINGE
K-Number: K091279 · 2009-08-12
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Device Summary
Frequently Asked Questions
What is the NIPRO DISPOSABLE SYRINGE?
NIPRO DISPOSABLE SYRINGE is a medical device that received FDA 510(k) clearance on 2009-08-12. The listed applicant is Nipro Medical Corporation. The 510(k) number is K091279.
When did NIPRO DISPOSABLE SYRINGE receive FDA 510(k) clearance?
NIPRO DISPOSABLE SYRINGE received FDA 510(k) clearance on 2009-08-12, under 510(k) number K091279.
Who is the listed applicant for NIPRO DISPOSABLE SYRINGE?
The FDA 510(k) record lists Nipro Medical Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIPRO DISPOSABLE SYRINGE?
The FDA product code for NIPRO DISPOSABLE 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 Corporation 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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