meddevicedb.com FDA Device Reference

SPECTRA 1 FILTER PHOTOMETER

K850994 Class I Traditional
Decision Date
1985-05-10
Sponsor / Applicant
Awareness Technology, Inc.

Technical Specification

510(k) Submission ID K850994
Product Code JJQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2300
Decision Date 1985-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTRA 1 FILTER PHOTOMETER received FDA 510(k) clearance under submission number K850994, sponsored by Awareness Technology, 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 1985-05-10.

Classification & Regulation

This clearance is catalogued under FDA product code JJQ and 21 CFR 862.2300, within the Clinical Chemistry review panel as a Class I device.