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FDA 510(k)

BP-1000

K-Number: K843009 · 1984-08-24

Decision Date1984-08-24
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BP-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Pollenex Associated Mills, Inc.. It received FDA 510(k) clearance on 1984-08-24 under 510(k) number K843009. 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-1000?

BP-1000 is a medical device that received FDA 510(k) clearance on 1984-08-24. The listed applicant is Pollenex Associated Mills, Inc.. The 510(k) number is K843009.

When did BP-1000 receive FDA 510(k) clearance?

BP-1000 received FDA 510(k) clearance on 1984-08-24, under 510(k) number K843009.

Who is the listed applicant for BP-1000?

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

What is the FDA product code for BP-1000?

The FDA product code for BP-1000 is DXN.

Other records listing Pollenex Associated Mills, 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.

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

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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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