VAN DELLEN CANNULA
K-Number: K873464 · 1987-11-23
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Device Summary
Frequently Asked Questions
What is the VAN DELLEN CANNULA?
VAN DELLEN CANNULA is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Van Dellen, Ltd.. The 510(k) number is K873464.
When did VAN DELLEN CANNULA receive FDA 510(k) clearance?
VAN DELLEN CANNULA received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873464.
Who is the listed applicant for VAN DELLEN CANNULA?
The FDA 510(k) record lists Van Dellen, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAN DELLEN CANNULA?
The FDA product code for VAN DELLEN CANNULA is JOL.
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 Van Dellen, Ltd. 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: JOL)
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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