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FDA 510(k)

R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL

K-Number: K051339 · 2005-07-12

Decision Date2005-07-12
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is R&D Systems, Inc.. It received FDA 510(k) clearance on 2005-07-12 under 510(k) number K051339. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL?

R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 2005-07-12. The listed applicant is R&D Systems, Inc.. The 510(k) number is K051339.

When did R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL receive FDA 510(k) clearance?

R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL received FDA 510(k) clearance on 2005-07-12, under 510(k) number K051339.

Who is the listed applicant for R&D CBC-4K PLUS RETICS 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 R&D CBC-4K PLUS RETICS HEMATOLOGY CONTROL?

The FDA product code for R&D CBC-4K PLUS RETICS 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.

View all 79 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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