SURFAS

Transducer, Ultrasonic, Diagnostic

D.O. WEAVER AND CO.

The following data is part of a premarket notification filed by D.o. Weaver And Co. with the FDA for Surfas.

Pre-market Notification Details

• Device ID: K925081
• 510k Number: K925081
• Device Name: SURFAS
• Classification: Transducer, Ultrasonic, Diagnostic
• Applicant: D.O. WEAVER AND CO. 565-C NUCLA WAY Aurora, CO 80011
• Contact: Douglas T Cleveland
• Correspondent: Douglas T Cleveland; D.O. WEAVER AND CO. 565-C NUCLA WAY Aurora, CO 80011
• Product Code: ITX
• CFR Regulation Number: 892.1570 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-10-07
• Decision Date: 1993-09-28