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FDA 510(k)

TALON AND REVERE

K-Number: K071245 · 2007-08-02

ApplicantTalon Acrylics, Inc.
Decision Date2007-08-02
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TALON AND REVERE is the device name listed in this FDA 510(k) record. The listed applicant is Talon Acrylics, Inc.. It received FDA 510(k) clearance on 2007-08-02 under 510(k) number K071245. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TALON AND REVERE?

TALON AND REVERE is a medical device that received FDA 510(k) clearance on 2007-08-02. The listed applicant is Talon Acrylics, Inc.. The 510(k) number is K071245.

When did TALON AND REVERE receive FDA 510(k) clearance?

TALON AND REVERE received FDA 510(k) clearance on 2007-08-02, under 510(k) number K071245.

Who is the listed applicant for TALON AND REVERE?

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

What is the FDA product code for TALON AND REVERE?

The FDA product code for TALON AND REVERE is EBI.

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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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