AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION— 510(k) K992317

Name: FDA 510(k) clearance K992317
Creator: U.S. Food and Drug Administration
Published: 1999-10-01

Substantially Equivalent

Adac Laboratories

FDA 510(k) clearance K992317 for AUTOSPECT PLUS WITH INSTILL MOTION CORRECTION, Substantially Equivalent on 1999-10-01. Applicant: Adac Laboratories. Device class: 2.

Clearance details

Applicant: Adac Laboratories
Product code: Code KPS
Device class: Class 2
Regulation: 21 CFR 892.1200
Advisory panel: Radiology
Date received: 1999-07-09
Decision date: 1999-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, CA, US

Download summary PDF View on FDA.gov ↗

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