SEGMENT

System, Image Processing, Radiological

MEDVISO

The following data is part of a premarket notification filed by Medviso with the FDA for Segment.

Pre-market Notification Details

• Device ID: K090833
• 510k Number: K090833
• Device Name: SEGMENT
• Classification: System, Image Processing, Radiological
• Applicant: MEDVISO THULEHEMSVAGEN 157 Lund, SE Se-22467
• Contact: Einar Heiberg
• Correspondent: Einar Heiberg; MEDVISO THULEHEMSVAGEN 157 Lund, SE Se-22467
• Product Code: LLZ
• CFR Regulation Number: 892.2050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2009-03-26
• Decision Date: 2009-05-12
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
07350010100010	K090833	000