MWX-7440 HIGH SPEED BUCKY— 510(k) K924423

Name: FDA 510(k) clearance K924423
Creator: U.S. Food and Drug Administration
Published: 1993-01-15

Substantially Equivalent

Midwest X-Ray Equipment Co.

FDA 510(k) clearance K924423 for MWX-7440 HIGH SPEED BUCKY, Substantially Equivalent on 1993-01-15. Applicant: Midwest X-Ray Equipment Co.. Device class: 2.

Clearance details

Applicant: Midwest X-Ray Equipment Co.
Product code: Code KPX
Device class: Class 2
Regulation: 21 CFR 892.1860
Advisory panel: Radiology
Date received: 1992-09-01
Decision date: 1993-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Aurora, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPX

view all

K945635 — TRANS X-10001995-02-01
K935157 — ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES1994-08-09
K934850 — NUCLEAR ASSOCIATES PERSONNEL PROTECTIVE SHIELDS1993-11-22
K933035 — BCM-600TX1993-10-08
K925598 — BUCKYMATIC AUTOMATIC CHEST FILM CHANGER1993-02-01

More clearances from Midwest X-Ray Equipment Co.

view all

K827609 — MIDWEST AUTOMATIC BUCKY EQUIPPED WITH GRID AND SIZE-O-MATIC TRAY1982-07-09
K827504 — SIZE SENSING CASSETTE TRAY1982-06-09

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