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FDA 510(k)

PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST

K-Number: K932921 · 1993-08-30

Decision Date1993-08-30
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS INTRODUCER FOR VENA CAVA FILTER SYST is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun Vena-Tech. It received FDA 510(k) clearance on 1993-08-30 under 510(k) number K932921. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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