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OPACIDEN OPA REAGENT STRIPS

K070419 Class II Traditional
Decision Date
2007-08-31
Sponsor / Applicant
Hach Company

Technical Specification

510(k) Submission ID K070419
Product Code JOJ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2800
Decision Date 2007-08-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPACIDEN OPA REAGENT STRIPS received FDA 510(k) clearance under submission number K070419, sponsored by Hach Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2007-08-31.

Classification & Regulation

This clearance is catalogued under FDA product code JOJ and 21 CFR 880.2800, within the General Hospital review panel as a Class II device.