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RE-ENTRANT CHAMBER, MODEL 1008 OR 44D

K002446 Class II Traditional
Decision Date
2000-10-23
Sponsor / Applicant
Sun Nuclear Corp.

Technical Specification

510(k) Submission ID K002446
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2000-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RE-ENTRANT CHAMBER, MODEL 1008 OR 44D received FDA 510(k) clearance under submission number K002446, sponsored by Sun Nuclear Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2000-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.