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RETIC CHEX LINEARITY

K000115 Class II Traditional
Decision Date
2000-03-27
Sponsor / Applicant
Streck Laboratories, Inc.

Technical Specification

510(k) Submission ID K000115
Product Code JPK
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.8625
Decision Date 2000-03-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RETIC CHEX LINEARITY received FDA 510(k) clearance under submission number K000115, sponsored by Streck Laboratories, 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 2000-03-27.

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.