FDA 510(k)

PALM BLADDER SCANNER

K-Number: K130229 · 2013-03-20

ApplicantMianyang Meike Electronic Equipment Co., Ltd.

Decision Date2013-03-20

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PALM BLADDER SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Mianyang Meike Electronic Equipment Co., Ltd.. It received FDA 510(k) clearance on 2013-03-20 under 510(k) number K130229. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PALM BLADDER SCANNER?

PALM BLADDER SCANNER is a medical device that received FDA 510(k) clearance on 2013-03-20. The listed applicant is Mianyang Meike Electronic Equipment Co., Ltd.. The 510(k) number is K130229.

When did PALM BLADDER SCANNER receive FDA 510(k) clearance?

PALM BLADDER SCANNER received FDA 510(k) clearance on 2013-03-20, under 510(k) number K130229.

Who is the listed applicant for PALM BLADDER SCANNER?

The FDA 510(k) record lists Mianyang Meike Electronic Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PALM BLADDER SCANNER?

The FDA product code for PALM BLADDER SCANNER is IYO.

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Other records listing Mianyang Meike Electronic Equipment Co., Ltd. as applicant

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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.