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FDA 510(k)

POC-AS10 AUTO SAMPLER

K-Number: K092817 · 2010-03-09

ApplicantOtsuka Pharmaceutical Co., Ltd.
Decision Date2010-03-09
Product CodeMSQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

POC-AS10 AUTO SAMPLER is the device name listed in this FDA 510(k) record. The listed applicant is Otsuka Pharmaceutical Co., Ltd.. It received FDA 510(k) clearance on 2010-03-09 under 510(k) number K092817. The device is classified under product code MSQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POC-AS10 AUTO SAMPLER?

POC-AS10 AUTO SAMPLER is a medical device that received FDA 510(k) clearance on 2010-03-09. The listed applicant is Otsuka Pharmaceutical Co., Ltd.. The 510(k) number is K092817.

When did POC-AS10 AUTO SAMPLER receive FDA 510(k) clearance?

POC-AS10 AUTO SAMPLER received FDA 510(k) clearance on 2010-03-09, under 510(k) number K092817.

Who is the listed applicant for POC-AS10 AUTO SAMPLER?

The FDA 510(k) record lists Otsuka Pharmaceutical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POC-AS10 AUTO SAMPLER?

The FDA product code for POC-AS10 AUTO SAMPLER is MSQ.

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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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