ULTIMETER

Instrument, Quality-assurance, Radiologic

RADIATION MEASUREMENTS, INC.

The following data is part of a premarket notification filed by Radiation Measurements, Inc. with the FDA for Ultimeter.

Pre-market Notification Details

• Device ID: K873956
• 510k Number: K873956
• Device Name: ULTIMETER
• Classification: Instrument, Quality-assurance, Radiologic
• Applicant: RADIATION MEASUREMENTS, INC. P.O. BOX 327 7617 DONNA DRIVE Middleton, WI 53562
• Contact: Joel R Schenck
• Correspondent: Joel R Schenck; RADIATION MEASUREMENTS, INC. P.O. BOX 327 7617 DONNA DRIVE Middleton, WI 53562
• Product Code: LHO
• CFR Regulation Number: 892.1940 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1987-09-28
• Decision Date: 1987-10-30