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SPECTROPHOTOMETER ANALYSIS SYS., AA-375

K770444 Class I Traditional
Decision Date
1977-04-08
Sponsor / Applicant
Varian Assoc., Inc.

Technical Specification

510(k) Submission ID K770444
Product Code JXR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2850
Decision Date 1977-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTROPHOTOMETER ANALYSIS SYS., AA-375 received FDA 510(k) clearance under submission number K770444, sponsored by Varian Assoc., 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 1977-04-08.

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.