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PHO. TRAX MODEL 4000 WHOLE BODY SCAN.

K760808 Class II Traditional
Decision Date
1976-11-05
Sponsor / Applicant
G.D. Searle and Co.

Technical Specification

510(k) Submission ID K760808
Product Code JAK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1750
Decision Date 1976-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHO. TRAX MODEL 4000 WHOLE BODY SCAN. received FDA 510(k) clearance under submission number K760808, sponsored by G.D. Searle and Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1976-11-05.

Classification & Regulation

This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.