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SOLID PHASE BOIL DUALCOUNT (DUALCOUNT SPB)

K860815 Class II Traditional
Decision Date
1986-07-11
Sponsor / Applicant
Diagnostic Products Corp.

Technical Specification

510(k) Submission ID K860815
Product Code CDD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1810
Decision Date 1986-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOLID PHASE BOIL DUALCOUNT (DUALCOUNT SPB) received FDA 510(k) clearance under submission number K860815, sponsored by Diagnostic Products Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1986-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code CDD and 21 CFR 862.1810, within the Clinical Chemistry review panel as a Class II device.