INTERAD 520— 510(k) K833821

Substantially Equivalent

Interad Systems, Inc.

FDA 510(k) clearance K833821 for INTERAD 520, Substantially Equivalent on 1984-01-13. Applicant: Interad Systems, Inc.. Device class: 1.

Clearance details

Applicant: Interad Systems, Inc.
Product code: Code IYX
Device class: Class 1
Regulation: 21 CFR 892.1100
Advisory panel: Radiology
Date received: 1983-11-02
Decision date: 1984-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IYX

K230221 — QDOSE® Multi-purpose Voxel Dosimetry (Personalized Dosimetry in Molecular Radiotherapy)2023-08-28
K212587 — 3D-RD-S2023-02-22
K163687 — OLINDA EXM2017-07-19
K160933 — Discovery NM 750b Bopsy2016-11-18
K162052 — Sentinella 102, Sentinella 102 Horus2016-08-18

More clearances from Interad Systems, Inc.

K834087 — MODEL XLE1984-02-27
K834307 — ULTRASOUND SCANNER XL1984-02-21
K813162 — INTERAD WHOLE BODY CT SCANNER1981-12-14

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