CENTRALITE BACKPOINTER— 510(k) K893398

Substantially Equivalent

Diacor, Inc.

FDA 510(k) clearance K893398 for CENTRALITE BACKPOINTER, Substantially Equivalent on 1989-08-17. 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: 1989-05-01
Decision date: 1989-08-17
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.