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R&D 5D RETIC HEMATOLOGY CONTROL

K130962 Class II Special
Decision Date
2013-07-24
Sponsor / Applicant
R&D Systems, Inc.

Technical Specification

510(k) Submission ID K130962
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2013-07-24
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

R&D 5D RETIC HEMATOLOGY CONTROL received FDA 510(k) clearance under submission number K130962, sponsored by R&D Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2013-07-24.

Classification & Regulation

This clearance is catalogued under FDA product code JPK and 21 CFR 864.8625, within the Hematology review panel as a Class II device.