CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL
K-Number: K850755 · 1985-05-13
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Device Summary
Frequently Asked Questions
What is the CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL?
CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is R&D Systems, Inc.. The 510(k) number is K850755.
When did CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL receive FDA 510(k) clearance?
CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL received FDA 510(k) clearance on 1985-05-13, under 510(k) number K850755.
Who is the listed applicant for CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL?
The FDA 510(k) record lists R&D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL?
The FDA product code for CBC-PLT-4/MULTIPLE WHOLE BLOOD HEMATOLOGY CONTROL is JPK.
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 R&D Systems, Inc. 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: JPK)
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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