MAGNUM

Table, Physical Therapy, Multi Function

MAGNUM EQUIPMENT L.L.C.

The following data is part of a premarket notification filed by Magnum Equipment L.l.c. with the FDA for Magnum.

Pre-market Notification Details

• Device ID: K010252
• 510k Number: K010252
• Device Name: MAGNUM
• Classification: Table, Physical Therapy, Multi Function
• Applicant: MAGNUM EQUIPMENT L.L.C. 7222 W. MELROSE LN. Oklahoma City, OK 73127
• Contact: Monte Regal
• Correspondent: Monte Regal; MAGNUM EQUIPMENT L.L.C. 7222 W. MELROSE LN. Oklahoma City, OK 73127
• Product Code: JFB
• CFR Regulation Number: 890.5880 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2001-01-26
• Decision Date: 2001-04-26