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FDA 510(k)

BP652N (HEM-6300-Z)

K-Number: K123498 · 2013-03-21

Decision Date2013-03-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP652N (HEM-6300-Z) is the device name listed in this FDA 510(k) record. The listed applicant is Omron Healthcare, Inc.. It received FDA 510(k) clearance on 2013-03-21 under 510(k) number K123498. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BP652N (HEM-6300-Z)?

BP652N (HEM-6300-Z) is a medical device that received FDA 510(k) clearance on 2013-03-21. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K123498.

When did BP652N (HEM-6300-Z) receive FDA 510(k) clearance?

BP652N (HEM-6300-Z) received FDA 510(k) clearance on 2013-03-21, under 510(k) number K123498.

Who is the listed applicant for BP652N (HEM-6300-Z)?

The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP652N (HEM-6300-Z)?

The FDA product code for BP652N (HEM-6300-Z) is DXN.

Other records listing Omron Healthcare, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 63 devices →

Related Devices (Code: DXN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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