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FDA 510(k)

BellaFuse

K-Number: K151271 · 2016-03-11

ApplicantHans Biomed Corp.
Decision Date2016-03-11
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BellaFuse is a medical device manufactured by Hans Biomed Corp.. It received FDA 510(k) clearance on 2016-03-11 under approval number K151271. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BellaFuse?

BellaFuse is a medical device that received FDA 510(k) clearance on 2016-03-11. It is manufactured by Hans Biomed Corp.. The 510(k) number is K151271.

When was BellaFuse approved by the FDA?

BellaFuse received FDA 510(k) clearance on 2016-03-11, under approval number K151271.

What company makes BellaFuse?

BellaFuse is manufactured by Hans Biomed Corp..

What is the FDA product code for BellaFuse?

The FDA product code for BellaFuse is MQV.

Other Devices by Hans Biomed Corp.

K152077MaxiGen

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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