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8700 CLINICAL CHEM. ANALYZER

K820888 Class I Traditional
Decision Date
1982-05-14
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K820888
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 1982-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

8700 CLINICAL CHEM. ANALYZER received FDA 510(k) clearance under submission number K820888, 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 1982-05-14.

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.