NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES— 510(k) K971167

Name: FDA 510(k) clearance K971167
Creator: U.S. Food and Drug Administration
Published: 1997-06-26

Substantially Equivalent

Neoprobe Corp.

FDA 510(k) clearance K971167 for NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES, Substantially Equivalent on 1997-06-26. Applicant: Neoprobe Corp.. Device class: 1.

Clearance details

Applicant: Neoprobe Corp.
Product code: Code IZD
Device class: Class 1
Regulation: 21 CFR 892.1320
Advisory panel: Radiology
Date received: 1997-03-31
Decision date: 1997-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, OH, US

Download summary PDF View on FDA.gov ↗

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