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PROBE, UPTAKE, NUCLEAR

K864624 Class I Traditional
Decision Date
1987-08-10
Sponsor / Applicant
Carolina Medical Electronics

Technical Specification

510(k) Submission ID K864624
Product Code IZO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1700
Decision Date 1987-08-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROBE, UPTAKE, NUCLEAR received FDA 510(k) clearance under submission number K864624, sponsored by Carolina Medical Electronics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1987-08-10.

Classification & Regulation

This clearance is catalogued under FDA product code IZO and 21 CFR 892.1700, within the Radiology review panel as a Class I device.