PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST
K-Number: K932921 · 1993-08-30
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Device Summary
Frequently Asked Questions
What is the PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST?
PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST is a medical device that received FDA 510(k) clearance on 1993-08-30. The listed applicant is B. Braun Vena-Tech. The 510(k) number is K932921.
When did PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST receive FDA 510(k) clearance?
PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST received FDA 510(k) clearance on 1993-08-30, under 510(k) number K932921.
Who is the listed applicant for PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST?
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 PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST?
The FDA product code for PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST 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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