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FDA 510(k)

BP-200 PLUS

K-Number: K063814 · 2007-03-07

ApplicantSchiller AG
Decision Date2007-03-07
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP-200 PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Schiller AG. It received FDA 510(k) clearance on 2007-03-07 under 510(k) number K063814. 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 BP-200 PLUS?

BP-200 PLUS is a medical device that received FDA 510(k) clearance on 2007-03-07. The listed applicant is Schiller AG. The 510(k) number is K063814.

When did BP-200 PLUS receive FDA 510(k) clearance?

BP-200 PLUS received FDA 510(k) clearance on 2007-03-07, under 510(k) number K063814.

Who is the listed applicant for BP-200 PLUS?

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

What is the FDA product code for BP-200 PLUS?

The FDA product code for BP-200 PLUS is DXN.

Other records listing Schiller AG as applicant

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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.

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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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