CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY
K-Number: K852371 · 1985-09-17
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Device Summary
Frequently Asked Questions
What is the CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY?
CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY is a medical device that received FDA 510(k) clearance on 1985-09-17. The listed applicant is Abbott Diagnostics. The 510(k) number is K852371.
When did CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY receive FDA 510(k) clearance?
CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY received FDA 510(k) clearance on 1985-09-17, under 510(k) number K852371.
Who is the listed applicant for CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY?
The FDA 510(k) record lists Abbott Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY?
The FDA product code for CELL-DYN 2000 AUTOMATED MULTI-PARAMETER HEMATOLOGY 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 Abbott Diagnostics 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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