PHARMASEED, MODEL BT-125-2— 510(k) K993701

Name: FDA 510(k) clearance K993701
Creator: U.S. Food and Drug Administration
Published: 2000-06-09

Substantially Equivalent

Syncor International, Inc.

FDA 510(k) clearance K993701 for PHARMASEED, MODEL BT-125-2, Substantially Equivalent on 2000-06-09. Applicant: Syncor International, Inc.. Device class: 2.

Clearance details

Applicant: Syncor International, Inc.
Product code: Code KXK
Device class: Class 2
Regulation: 21 CFR 892.5730
Advisory panel: Radiology
Date received: 1999-11-02
Decision date: 2000-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Golden, CO, US

Download summary PDF View on FDA.gov ↗

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