NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES— 510(k) K942580

Name: FDA 510(k) clearance K942580
Creator: U.S. Food and Drug Administration
Published: 1995-02-09

Substantially Equivalent

Neoprobe Corp.

FDA 510(k) clearance K942580 for NEOPROBE 1000 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIES, Substantially Equivalent on 1995-02-09. 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: 1994-05-31
Decision date: 1995-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dublin, OH, US

Download summary PDF View on FDA.gov ↗

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