Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

R&D LH-NRBC HEMATOLOGY CONTROL

K-Number: K061320 · 2006-06-02

Decision Date2006-06-02
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

R&D LH-NRBC 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 2006-06-02 under 510(k) number K061320. 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 LH-NRBC HEMATOLOGY CONTROL?

R&D LH-NRBC HEMATOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 2006-06-02. The listed applicant is R&D Systems, Inc.. The 510(k) number is K061320.

When did R&D LH-NRBC HEMATOLOGY CONTROL receive FDA 510(k) clearance?

R&D LH-NRBC HEMATOLOGY CONTROL received FDA 510(k) clearance on 2006-06-02, under 510(k) number K061320.

Who is the listed applicant for R&D LH-NRBC 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 LH-NRBC HEMATOLOGY CONTROL?

The FDA product code for R&D LH-NRBC 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

View on FDA Database →

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

↑