IQ SYSTEM

Plethysmograph, Impedance

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: K981720
• 510k Number: K981720
• Device Name: IQ SYSTEM
• Classification: Plethysmograph, Impedance
• Applicant: RENAISSANCE TECHNOLOGY, INC. 170 PHEASANT RUN Newtown, PA 18940
• Contact: Philip E Hamski
• Correspondent: Philip E Hamski; RENAISSANCE TECHNOLOGY, INC. 170 PHEASANT RUN Newtown, PA 18940
• Product Code: DSB
• CFR Regulation Number: 870.2770 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1998-05-05
• Decision Date: 1999-02-08