SENTEC LASER GUIDE LINE, MODEL SGL-05— 510(k) K862340

Name: FDA 510(k) clearance K862340
Creator: U.S. Food and Drug Administration
Published: 1986-07-11

Substantially Equivalent

Sentec Corp.

FDA 510(k) clearance K862340 for SENTEC LASER GUIDE LINE, MODEL SGL-05, Substantially Equivalent on 1986-07-11. Applicant: Sentec Corp.. Device class: 2.

Clearance details

Applicant: Sentec Corp.
Product code: Code IZW
Device class: Class 2
Regulation: 21 CFR 892.1610
Advisory panel: Radiology
Date received: 1986-06-20
Decision date: 1986-07-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Birmingham, MI, US

Download summary PDF View on FDA.gov ↗

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