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FDA 510(k)

HEMATOLOGY REFERENCE CONTROLS

K-Number: K772195 · 1978-02-03

Decision Date1978-02-03
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HEMATOLOGY REFERENCE CONTROLS 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 1978-02-03 under 510(k) number K772195. 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 HEMATOLOGY REFERENCE CONTROLS?

HEMATOLOGY REFERENCE CONTROLS is a medical device that received FDA 510(k) clearance on 1978-02-03. The listed applicant is R&D Systems, Inc.. The 510(k) number is K772195.

When did HEMATOLOGY REFERENCE CONTROLS receive FDA 510(k) clearance?

HEMATOLOGY REFERENCE CONTROLS received FDA 510(k) clearance on 1978-02-03, under 510(k) number K772195.

Who is the listed applicant for HEMATOLOGY REFERENCE CONTROLS?

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 HEMATOLOGY REFERENCE CONTROLS?

The FDA product code for HEMATOLOGY REFERENCE CONTROLS 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.

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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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