TITANIUM GREENFIELD VENA CAVA FILTER CARRIER
K-Number: K874096 · 1988-11-04
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Device Summary
Frequently Asked Questions
What is the TITANIUM GREENFIELD VENA CAVA FILTER CARRIER?
TITANIUM GREENFIELD VENA CAVA FILTER CARRIER is a medical device that received FDA 510(k) clearance on 1988-11-04. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K874096.
When did TITANIUM GREENFIELD VENA CAVA FILTER CARRIER receive FDA 510(k) clearance?
TITANIUM GREENFIELD VENA CAVA FILTER CARRIER received FDA 510(k) clearance on 1988-11-04, under 510(k) number K874096.
Who is the listed applicant for TITANIUM GREENFIELD VENA CAVA FILTER CARRIER?
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 GREENFIELD VENA CAVA FILTER CARRIER?
The FDA product code for TITANIUM GREENFIELD VENA CAVA FILTER CARRIER 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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