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FDA 510(k)

AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS

K-Number: K925274 · 1994-09-30

Decision Date1994-09-30
Product CodeGKZ
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Immunocytometry Systems. It received FDA 510(k) clearance on 1994-09-30 under 510(k) number K925274. 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 AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS?

AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS is a medical device that received FDA 510(k) clearance on 1994-09-30. The listed applicant is Becton Dickinson Immunocytometry Systems. The 510(k) number is K925274.

When did AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS receive FDA 510(k) clearance?

AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS received FDA 510(k) clearance on 1994-09-30, under 510(k) number K925274.

Who is the listed applicant for AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS?

The FDA 510(k) record lists Becton Dickinson Immunocytometry Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS?

The FDA product code for AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS 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 Becton Dickinson Immunocytometry Systems 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 21 devices →

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

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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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