RADKOR XG-325— 510(k) K881696

Substantially Equivalent

Radkor, Inc.

FDA 510(k) clearance K881696 for RADKOR XG-325, Substantially Equivalent on 1988-09-02. Applicant: Radkor, Inc.. Device class: 1.

Clearance details

Applicant: Radkor, Inc.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1988-04-19
Decision date: 1988-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZO

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K952265 — MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR1995-07-06

More clearances from Radkor, Inc.

K895969 — RADKOR DXG-650R1989-11-13
K892196 — RADKOR TS10-B1989-04-26
K891395 — RADKOR BS-10 AND BS-10T1989-04-03
K883864 — RADKOR SFR-701988-10-19
K883885 — RADKOR, RF-1591988-10-19

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