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FDA 510(k)

BD FACSCANTO WITH BD FACSANTO SOFTWARE

K-Number: K041074 · 2004-09-17

Decision Date2004-09-17
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BD FACSCANTO WITH BD FACSANTO SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Biosciences. It received FDA 510(k) clearance on 2004-09-17 under 510(k) number K041074. The device is classified under product code GKZ. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD FACSCANTO WITH BD FACSANTO SOFTWARE?

BD FACSCANTO WITH BD FACSANTO SOFTWARE is a medical device that received FDA 510(k) clearance on 2004-09-17. The listed applicant is Bd Biosciences. The 510(k) number is K041074.

When did BD FACSCANTO WITH BD FACSANTO SOFTWARE receive FDA 510(k) clearance?

BD FACSCANTO WITH BD FACSANTO SOFTWARE received FDA 510(k) clearance on 2004-09-17, under 510(k) number K041074.

Who is the listed applicant for BD FACSCANTO WITH BD FACSANTO SOFTWARE?

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

What is the FDA product code for BD FACSCANTO WITH BD FACSANTO SOFTWARE?

The FDA product code for BD FACSCANTO WITH BD FACSANTO SOFTWARE is GKZ.

Related Clinical Trials

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.

Other records listing Bd Biosciences 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.

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Related Devices (Code: GKZ)

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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