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FDA 510(k)

THYROSAMPLER

K-Number: K062979 · 2007-05-30

ApplicantAcd Medical Innovation Corp.
Decision Date2007-05-30
Product CodeFCG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

THYROSAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Acd Medical Innovation Corp.. It received FDA 510(k) clearance on 2007-05-30 under 510(k) number K062979. The device is classified under product code FCG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYROSAMPLER?

THYROSAMPLER is a medical device that received FDA 510(k) clearance on 2007-05-30. The listed applicant is Acd Medical Innovation Corp.. The 510(k) number is K062979.

When did THYROSAMPLER receive FDA 510(k) clearance?

THYROSAMPLER received FDA 510(k) clearance on 2007-05-30, under 510(k) number K062979.

Who is the listed applicant for THYROSAMPLER?

The FDA 510(k) record lists Acd Medical Innovation Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THYROSAMPLER?

The FDA product code for THYROSAMPLER is FCG.

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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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