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ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB

K810536 Class I Traditional
Decision Date
1981-03-17
Sponsor / Applicant
The Perkin-Elmer Corp.

Technical Specification

510(k) Submission ID K810536
Product Code JXR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2850
Decision Date 1981-03-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ZEEMAN/5000 GRAPHITE FURNACE ATOMIC ABSB received FDA 510(k) clearance under submission number K810536, sponsored by The Perkin-Elmer 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 1981-03-17.

Classification & Regulation

This clearance is catalogued under FDA product code JXR and 21 CFR 862.2850, within the Clinical Chemistry review panel as a Class I device.