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BOOMERANG ABSORPTION COMENSATION FILTER

K853330 Class II Traditional
Decision Date
1985-11-15
Sponsor / Applicant
Entreprises Octostop, Inc.

Technical Specification

510(k) Submission ID K853330
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 1985-11-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOOMERANG ABSORPTION COMENSATION FILTER received FDA 510(k) clearance under submission number K853330, sponsored by Entreprises Octostop, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1985-11-15.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.