ALTAIREX BUCKY/CASSETTE TRAY COMBINATION— 510(k) K873849

Name: FDA 510(k) clearance K873849
Creator: U.S. Food and Drug Administration
Published: 1987-10-28

Substantially Equivalent

Altairex Manufacturing, Inc.

FDA 510(k) clearance K873849 for ALTAIREX BUCKY/CASSETTE TRAY COMBINATION, Substantially Equivalent on 1987-10-28. Applicant: Altairex Manufacturing, Inc.. Device class: 2.

Clearance details

Applicant: Altairex Manufacturing, Inc.
Product code: Code IXQ
Device class: Class 2
Regulation: 21 CFR 892.1980
Advisory panel: Radiology
Date received: 1987-09-22
Decision date: 1987-10-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Boulder, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXQ

view all

K973842 — CARBON FIBER CONFORMAL COUCH TOP1997-12-05
K960083 — MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 3001996-07-24
K954225 — MED-TEC HAND GRIP1995-11-14
K946262 — EURO, SCST, SCCFT ATLAS RADIOLOGIC TABLES1995-02-15
K942916 — OCTOPAQUE UNIVERSAL1994-09-08

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