NEOPROBE PORTABLE RADIOSCOPE DETECTOR— 510(k) K915279

Name: FDA 510(k) clearance K915279
Creator: U.S. Food and Drug Administration
Published: 1992-06-10

Substantially Equivalent

Neoprobe Corp.

FDA 510(k) clearance K915279 for NEOPROBE PORTABLE RADIOSCOPE DETECTOR, Substantially Equivalent on 1992-06-10. 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: 1991-11-25
Decision date: 1992-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZD

view all

K133781 — DECLIPSESPECT LAPAROSCOPY2014-04-11
K123917 — DECLIPSESPECT VIEWER2013-01-25
K101887 — CONFIDENT SURGERY SUITE 300, MODEL CSS3002011-03-22
K013751 — HANDHELD GAMMA FINDER (HGF)2002-02-06
K983768 — MODIFICATION TO GAMMA GUIDANCE SYSTEM1999-07-02

More clearances from Neoprobe Corp.

view all

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