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BIOMEDICS BLADDER SCANNER

K842687 Class II Traditional
Decision Date
1985-04-08
Sponsor / Applicant
Biomedics

Technical Specification

510(k) Submission ID K842687
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 1985-04-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOMEDICS BLADDER SCANNER received FDA 510(k) clearance under submission number K842687, sponsored by Biomedics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1985-04-08.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.