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FDA 510(k)

MSI-HC HEMATOLOGY CONTROL

K-Number: K834043 · 1984-01-03

Decision Date1984-01-03
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MSI-HC HEMATOLOGY CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Specialties, Inc.. It received FDA 510(k) clearance on 1984-01-03 under 510(k) number K834043. 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 MSI-HC HEMATOLOGY CONTROL?

MSI-HC HEMATOLOGY CONTROL is a medical device that received FDA 510(k) clearance on 1984-01-03. The listed applicant is Medical Specialties, Inc.. The 510(k) number is K834043.

When did MSI-HC HEMATOLOGY CONTROL receive FDA 510(k) clearance?

MSI-HC HEMATOLOGY CONTROL received FDA 510(k) clearance on 1984-01-03, under 510(k) number K834043.

Who is the listed applicant for MSI-HC HEMATOLOGY CONTROL?

The FDA 510(k) record lists Medical Specialties, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MSI-HC HEMATOLOGY CONTROL?

The FDA product code for MSI-HC 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 Medical Specialties, 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 40 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.

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