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FDA 510(k)

ALCOHOL PAD

K-Number: K080466 · 2008-10-21

Applicant122 Corporation
Decision Date2008-10-21
Product CodeQBP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALCOHOL PAD is the device name listed in this FDA 510(k) record. The listed applicant is 122 Corporation. It received FDA 510(k) clearance on 2008-10-21 under 510(k) number K080466. The device is classified under product code QBP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCOHOL PAD?

ALCOHOL PAD is a medical device that received FDA 510(k) clearance on 2008-10-21. The listed applicant is 122 Corporation. The 510(k) number is K080466.

When did ALCOHOL PAD receive FDA 510(k) clearance?

ALCOHOL PAD received FDA 510(k) clearance on 2008-10-21, under 510(k) number K080466.

Who is the listed applicant for ALCOHOL PAD?

The FDA 510(k) record lists 122 Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALCOHOL PAD?

The FDA product code for ALCOHOL PAD is QBP.

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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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