CENTRALITE BACKPOINTER— 510(k) K954414

Substantially Equivalent

Diacor, Inc.

FDA 510(k) clearance K954414 for CENTRALITE BACKPOINTER, Substantially Equivalent on 1995-10-23. 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: 1995-09-21
Decision date: 1995-10-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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