TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER
K-Number: K870729 · 1987-04-09
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Device Summary
Frequently Asked Questions
What is the TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER?
TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER is a medical device that received FDA 510(k) clearance on 1987-04-09. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K870729.
When did TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER receive FDA 510(k) clearance?
TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER received FDA 510(k) clearance on 1987-04-09, under 510(k) number K870729.
Who is the listed applicant for TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER?
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 TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER?
The FDA product code for TITANIUM PERCUTANEOUS GREENFIELD VENA CAVE FILTER 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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