MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR— 510(k) K952265

Name: FDA 510(k) clearance K952265
Creator: U.S. Food and Drug Administration
Published: 1995-07-06

Substantially Equivalent

Control-X, Inc.

FDA 510(k) clearance K952265 for MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATOR, Substantially Equivalent on 1995-07-06. Applicant: Control-X, Inc.. Device class: 1.

Clearance details

Applicant: Control-X, Inc.
Product code: Code IZO
Device class: Class 1
Regulation: 21 CFR 892.1700
Advisory panel: Radiology
Date received: 1995-05-15
Decision date: 1995-07-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbus, OH, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IZO

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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
K950883 — POLYDOROS SX 65 AND 801995-04-03

More clearances from Control-X, Inc.

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K920347 — TOP-X 650HF RADIOGRAPHIC X-RAY1993-05-17
K924445 — BA-4 WALL BUCKY AND BA-42 TILTING WALL BUCKY1993-02-19
K920349 — PCX 1050HF RADIOGRAPHIC X-RAY GENERATOR1993-02-12
K920351 — PCX 650HF RADIOGRAPHIC X-RAY1993-02-12
K924443 — RS-3 UNIVERSAL RADIOGRAPHIC WORKING PLACE1993-02-05

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