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MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE

K903647 Class I Traditional
Decision Date
1990-09-11
Sponsor / Applicant
Millipore Corp.

Technical Specification

510(k) Submission ID K903647
Product Code LDM
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2260
Decision Date 1990-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODULE 486 VARIABLE WAVELENGTH TUNABLE UV/VIS DETE received FDA 510(k) clearance under submission number K903647, sponsored by Millipore 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 1990-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code LDM and 21 CFR 862.2260, within the Clinical Chemistry review panel as a Class I device.