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FDA 510(k)

BEL-CYPHER N

K-Number: K110160 · 2011-02-17

ApplicantTakara Belmont Corporation
Decision Date2011-02-17
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEL-CYPHER N is the device name listed in this FDA 510(k) record. The listed applicant is Takara Belmont Corporation. It received FDA 510(k) clearance on 2011-02-17 under 510(k) number K110160. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEL-CYPHER N?

BEL-CYPHER N is a medical device that received FDA 510(k) clearance on 2011-02-17. The listed applicant is Takara Belmont Corporation. The 510(k) number is K110160.

When did BEL-CYPHER N receive FDA 510(k) clearance?

BEL-CYPHER N received FDA 510(k) clearance on 2011-02-17, under 510(k) number K110160.

Who is the listed applicant for BEL-CYPHER N?

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

What is the FDA product code for BEL-CYPHER N?

The FDA product code for BEL-CYPHER N is MUH.

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Other records listing Takara Belmont Corporation as applicant

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Official Source

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