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MICROPLATE REAGENT DISPENSER

K900599 Class I Traditional
Decision Date
1990-05-17
Sponsor / Applicant
Denley Instruments, Inc.

Technical Specification

510(k) Submission ID K900599
Product Code JQW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2750
Decision Date 1990-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICROPLATE REAGENT DISPENSER received FDA 510(k) clearance under submission number K900599, sponsored by Denley Instruments, Inc.. 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 1990-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code JQW and 21 CFR 862.2750, within the Clinical Chemistry review panel as a Class I device.