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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 the device name listed in this FDA 510(k) record. The listed applicant is Hans Biomed Corp.. It received FDA 510(k) clearance on 2016-03-11 under 510(k) 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. The listed applicant is Hans Biomed Corp.. The 510(k) number is K151271.

When did BellaFuse receive FDA 510(k) clearance?

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

Who is the listed applicant for BellaFuse?

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

What is the FDA product code for BellaFuse?

The FDA product code for BellaFuse is MQV.

Other records listing Hans Biomed Corp. as applicant

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Related Devices (Code: MQV)

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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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