PLT - 4 PLATELET
K-Number: K840302 · 1984-03-12
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Device Summary
Frequently Asked Questions
What is the PLT - 4 PLATELET?
PLT - 4 PLATELET is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is R&D Systems, Inc.. The 510(k) number is K840302.
When did PLT - 4 PLATELET receive FDA 510(k) clearance?
PLT - 4 PLATELET received FDA 510(k) clearance on 1984-03-12, under 510(k) number K840302.
Who is the listed applicant for PLT - 4 PLATELET?
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 PLT - 4 PLATELET?
The FDA product code for PLT - 4 PLATELET 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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