IQ SYSTEM— 510(k) K922218

Substantially Equivalent

Renaissance Technology, Inc.

FDA 510(k) clearance K922218 for IQ SYSTEM, Substantially Equivalent on 1992-12-08. Applicant: Renaissance Technology, Inc.. Device class: 2.

Clearance details

Applicant: Renaissance Technology, Inc.
Product code: Code DXG
Device class: Class 2
Regulation: 21 CFR 870.1435
Advisory panel: Cardiovascular
Date received: 1992-05-12
Decision date: 1992-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newtown, PA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Renaissance Technology, Inc.

K981720 — IQ SYSTEM1999-02-08

Data sourced from openFDA. This site is unofficial and independent of the FDA.