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MICRODELTA, TC-99M-MAG3 RENAL PROCESSING PROGRAM

K905074 Class I Traditional
Decision Date
1991-06-21
Sponsor / Applicant
Siemens Gammasonics, Inc.

Technical Specification

510(k) Submission ID K905074
Product Code IYX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1100
Decision Date 1991-06-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MICRODELTA, TC-99M-MAG3 RENAL PROCESSING PROGRAM received FDA 510(k) clearance under submission number K905074, sponsored by Siemens Gammasonics, 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 1991-06-21.

Classification & Regulation

This clearance is catalogued under FDA product code IYX and 21 CFR 892.1100, within the Radiology review panel as a Class I device.