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FDA 510(k)

SAFEFLO VENA CAVA FILTER

K-Number: K081138 · 2009-05-07

ApplicantRmt Medical Technilogies, Inc.
Decision Date2009-05-07
Product CodeDTK
Advisory CommitteeCV
DecisionUnknown

Device Summary

SAFEFLO VENA CAVA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Rmt Medical Technilogies, Inc.. It received FDA 510(k) clearance on 2009-05-07 under 510(k) number K081138. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the SAFEFLO VENA CAVA FILTER?

SAFEFLO VENA CAVA FILTER is a medical device that received FDA 510(k) clearance on 2009-05-07. The listed applicant is Rmt Medical Technilogies, Inc.. The 510(k) number is K081138.

When did SAFEFLO VENA CAVA FILTER receive FDA 510(k) clearance?

SAFEFLO VENA CAVA FILTER received FDA 510(k) clearance on 2009-05-07, under 510(k) number K081138.

Who is the listed applicant for SAFEFLO VENA CAVA FILTER?

The FDA 510(k) record lists Rmt Medical Technilogies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFEFLO VENA CAVA FILTER?

The FDA product code for SAFEFLO VENA CAVA FILTER is DTK.

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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.

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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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