CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE
K-Number: K000897 · 2000-05-05
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Device Summary
Frequently Asked Questions
What is the CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE?
CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE is a medical device that received FDA 510(k) clearance on 2000-05-05. The listed applicant is Bd Biosciences. The 510(k) number is K000897.
When did CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE receive FDA 510(k) clearance?
CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE received FDA 510(k) clearance on 2000-05-05, under 510(k) number K000897.
Who is the listed applicant for CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP 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 CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP SOFTWARE?
The FDA product code for CALIBRITE PERCP-CY5.5 BEADS AND FACSCOMP 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.
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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