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MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15

K930544 Class II Traditional
Decision Date
1993-09-29
Sponsor / Applicant
Medrad, Inc.

Technical Specification

510(k) Submission ID K930544
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 1993-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 received FDA 510(k) clearance under submission number K930544, sponsored by Medrad, 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 1993-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.