AVITENE DISPENSER SYRINGE
K-Number: K924517 · 1993-10-27
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Device Summary
Frequently Asked Questions
What is the AVITENE DISPENSER SYRINGE?
AVITENE DISPENSER SYRINGE is a medical device that received FDA 510(k) clearance on 1993-10-27. The listed applicant is Nusurg, Inc.. The 510(k) number is K924517.
When did AVITENE DISPENSER SYRINGE receive FDA 510(k) clearance?
AVITENE DISPENSER SYRINGE received FDA 510(k) clearance on 1993-10-27, under 510(k) number K924517.
Who is the listed applicant for AVITENE DISPENSER SYRINGE?
The FDA 510(k) record lists Nusurg, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AVITENE DISPENSER SYRINGE?
The FDA product code for AVITENE DISPENSER SYRINGE is KYZ.
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 Nusurg, 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: KYZ)
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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