CANNULA, SURGICAL
K-Number: K903416 · 1990-11-23
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Device Summary
Frequently Asked Questions
What is the CANNULA, SURGICAL?
CANNULA, SURGICAL is a medical device that received FDA 510(k) clearance on 1990-11-23. The listed applicant is Advantage Diagnostics Corp.. The 510(k) number is K903416.
When did CANNULA, SURGICAL receive FDA 510(k) clearance?
CANNULA, SURGICAL received FDA 510(k) clearance on 1990-11-23, under 510(k) number K903416.
Who is the listed applicant for CANNULA, SURGICAL?
The FDA 510(k) record lists Advantage Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CANNULA, SURGICAL?
The FDA product code for CANNULA, SURGICAL is GEA.
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 Advantage Diagnostics 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: GEA)
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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