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PENN-PET SCANNER

K890100 Class II Traditional
Decision Date
1989-04-13
Sponsor / Applicant
Ugm Medical Systems, Inc.

Technical Specification

510(k) Submission ID K890100
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1989-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PENN-PET SCANNER received FDA 510(k) clearance under submission number K890100, sponsored by Ugm Medical Systems, 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 1989-04-13.

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.