CENTRALITE(R)-DLL SERIES— 510(k) K950112

Substantially Equivalent

Diacor, Inc.

FDA 510(k) clearance K950112 for CENTRALITE(R)-DLL SERIES, Substantially Equivalent on 1995-08-16. Applicant: Diacor, Inc.. Device class: 1.

Clearance details

Applicant: Diacor, Inc.
Product code: Code IWE
Device class: Class 1
Regulation: 21 CFR 892.5780
Advisory panel: Radiology
Date received: 1995-01-11
Decision date: 1995-08-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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