IQ SYSTEM

Computer, Diagnostic, Pre-programmed, Single-function

RENAISSANCE TECHNOLOGY, INC.

The following data is part of a premarket notification filed by Renaissance Technology, Inc. with the FDA for Iq System.

Pre-market Notification Details

• Device ID: K922218
• 510k Number: K922218
• Device Name: IQ SYSTEM
• Classification: Computer, Diagnostic, Pre-programmed, Single-function
• Applicant: RENAISSANCE TECHNOLOGY, INC. 31 FRIENDS LN. Newtown, PA 18940
• Contact: Philip E Hamski
• Correspondent: Philip E Hamski; RENAISSANCE TECHNOLOGY, INC. 31 FRIENDS LN. Newtown, PA 18940
• Product Code: DXG
• CFR Regulation Number: 870.1435 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1992-05-12
• Decision Date: 1992-12-08