PRISM

Bed, Flotation Therapy, Powered

BIO CLINIC CO.

The following data is part of a premarket notification filed by Bio Clinic Co. with the FDA for Prism.

Pre-market Notification Details

• Device ID: K932480
• 510k Number: K932480
• Device Name: PRISM
• Classification: Bed, Flotation Therapy, Powered
• Applicant: BIO CLINIC CO. 4083 E. AIRPORT DR. Ontario, CA 91761
• Contact: Greg Godfrey
• Correspondent: Greg Godfrey; BIO CLINIC CO. 4083 E. AIRPORT DR. Ontario, CA 91761
• Product Code: IOQ
• CFR Regulation Number: 890.5170 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-05-24
• Decision Date: 1993-07-21