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HGB-CONTROL SET/MULTIPLE

K893985 Class II Traditional
Decision Date
1989-08-15
Sponsor / Applicant
R&D Systems, Inc.

Technical Specification

510(k) Submission ID K893985
Product Code GGM
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 1989-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HGB-CONTROL SET/MULTIPLE received FDA 510(k) clearance under submission number K893985, sponsored by R&D Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1989-08-15.

Classification & Regulation

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