VENA CAVA FILTER SYSTEMS, MODIFICATION
K-Number: K925679 · 1992-11-27
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Device Summary
Frequently Asked Questions
What is the VENA CAVA FILTER SYSTEMS, MODIFICATION?
VENA CAVA FILTER SYSTEMS, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is B. Braun Vena-Tech. The 510(k) number is K925679.
When did VENA CAVA FILTER SYSTEMS, MODIFICATION receive FDA 510(k) clearance?
VENA CAVA FILTER SYSTEMS, MODIFICATION received FDA 510(k) clearance on 1992-11-27, under 510(k) number K925679.
Who is the listed applicant for VENA CAVA FILTER SYSTEMS, MODIFICATION?
The FDA 510(k) record lists B. Braun Vena-Tech as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENA CAVA FILTER SYSTEMS, MODIFICATION?
The FDA product code for VENA CAVA FILTER SYSTEMS, MODIFICATION is DTK.
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 B. Braun Vena-Tech 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: DTK)
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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