INFUSION CANNULA
K-Number: K942403 · 1994-08-17
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Device Summary
Frequently Asked Questions
What is the INFUSION CANNULA?
INFUSION CANNULA is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Microsurgical Technology, Inc.. The 510(k) number is K942403.
When did INFUSION CANNULA receive FDA 510(k) clearance?
INFUSION CANNULA received FDA 510(k) clearance on 1994-08-17, under 510(k) number K942403.
Who is the listed applicant for INFUSION CANNULA?
The FDA 510(k) record lists Microsurgical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INFUSION CANNULA?
The FDA product code for INFUSION CANNULA is HMX.
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 Microsurgical Technology, 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: HMX)
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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