AUTOCOMP(TM) SOFTWARE AND CALIBRITE(TM) BEADS
K-Number: K925274 · 1994-09-30
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Device Summary
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.
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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