PREMIUM

Mattress, Air Flotation, Alternating Pressure

KINETIC CONCEPTS, INC.

The following data is part of a premarket notification filed by Kinetic Concepts, Inc. with the FDA for Premium.

Pre-market Notification Details

• Device ID: K930673
• 510k Number: K930673
• Device Name: PREMIUM
• Classification: Mattress, Air Flotation, Alternating Pressure
• Applicant: KINETIC CONCEPTS, INC. 4958 STOUT DR. San Antonio, TX 78219
• Contact: William H Quirk
• Correspondent: William H Quirk; KINETIC CONCEPTS, INC. 4958 STOUT DR. San Antonio, TX 78219
• Product Code: FNM
• CFR Regulation Number: 880.5550 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1993-02-09
• Decision Date: 1993-08-02