ALPHA

Table, Radiographic, Non-tilting, Powered

RAYMAX MEDICAL CORP.

The following data is part of a premarket notification filed by Raymax Medical Corp. with the FDA for Alpha.

Pre-market Notification Details

• Device ID: K930273
• 510k Number: K930273
• Device Name: ALPHA
• Classification: Table, Radiographic, Non-tilting, Powered
• Applicant: RAYMAX MEDICAL CORP. 64 TROWERS ROAD WOODBRIDGE Ontario, L4l 7k5, CA
• Contact: Arvind Singh
• Correspondent: Arvind Singh; RAYMAX MEDICAL CORP. 64 TROWERS ROAD WOODBRIDGE Ontario, L4l 7k5, CA
• Product Code: IZZ
• CFR Regulation Number: 892.1980 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-01-19
• Decision Date: 1993-07-13