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TRANSCRAN(TM) TRANSCRANIAL PULSED DOPPLER SYSTEM

K882015 Class II Traditional
Decision Date
1988-09-08
Sponsor / Applicant
Ultramed, Inc.

Technical Specification

510(k) Submission ID K882015
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 1988-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSCRAN(TM) TRANSCRANIAL PULSED DOPPLER SYSTEM received FDA 510(k) clearance under submission number K882015, sponsored by Ultramed, 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 1988-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.