GEN-X 800/800— 510(k) K914301

Substantially Equivalent

Swissray Finatech, Inc.

FDA 510(k) clearance K914301 for GEN-X 800/800, Substantially Equivalent on 1991-10-30. Applicant: Swissray Finatech, Inc.. Device class: 1.

Clearance details

Applicant: Swissray Finatech, Inc.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1991-09-25
Decision date: 1991-10-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZO

K954666 — MPH50, MPH65, AND MPH801995-11-24
K953582 — HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATOR1995-09-26
K953831 — N 800 HF1995-09-08
K952822 — SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150G1995-07-12
K952265 — MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR1995-07-06

More clearances from Swissray Finatech, Inc.

K915339 — GEN-X 800/3001992-01-09
K914302 — GEN-X 800/6501991-10-30

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