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HERMES HDAQ ACQUISITION STATION AND HERMES WORKSTATION, VER. 3.4

K021656 Class II Special
Decision Date
2002-06-13
Sponsor / Applicant
Nuclear Diagnostics

Technical Specification

510(k) Submission ID K021656
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 2002-06-13
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HERMES HDAQ ACQUISITION STATION AND HERMES WORKSTATION, VER. 3.4 received FDA 510(k) clearance under submission number K021656, sponsored by Nuclear Diagnostics. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-06-13.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.