PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM
K-Number: K852097 · 1985-11-01
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Device Summary
Frequently Asked Questions
What is the PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM?
PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM is a medical device that received FDA 510(k) clearance on 1985-11-01. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K852097.
When did PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM receive FDA 510(k) clearance?
PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM received FDA 510(k) clearance on 1985-11-01, under 510(k) number K852097.
Who is the listed applicant for PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM?
The FDA 510(k) record lists Medi-Tech, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM?
The FDA product code for PERCUTANEOUS GREENFIELD VENA CAVA FILTER SYSTEM 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 Medi-Tech, Inc. 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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