ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION
K-Number: K972170 · 1997-07-24
Advertisement
Device Summary
Frequently Asked Questions
What is the ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION?
ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION is a medical device that received FDA 510(k) clearance on 1997-07-24. The listed applicant is R&D Systems, Inc.. The 510(k) number is K972170.
When did ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION receive FDA 510(k) clearance?
ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION received FDA 510(k) clearance on 1997-07-24, under 510(k) number K972170.
Who is the listed applicant for ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION?
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 ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION?
The FDA product code for ESR CONTROL-HC HEMATOLOGY ERYTHROCYTE SEDIMENTATION 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.
Advertisement