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ES600 IMMUNOASSAY SYSTEM

K860647 Class I Traditional
Decision Date
1986-04-17
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K860647
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1986-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ES600 IMMUNOASSAY SYSTEM received FDA 510(k) clearance under submission number K860647, sponsored by Boehringer Mannheim 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 1986-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.