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PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM

K052433 Class II Traditional
Decision Date
2005-10-18
Sponsor / Applicant
Bioptics, Inc.

Technical Specification

510(k) Submission ID K052433
Product Code MWP
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2005-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM received FDA 510(k) clearance under submission number K052433, sponsored by Bioptics, 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 2005-10-18.

Classification & Regulation

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