DIGITAL SUBTRACTION ANTIOGRAPHY PHANTOM 76-700/711— 510(k) K851812

Name: FDA 510(k) clearance K851812
Creator: U.S. Food and Drug Administration
Published: 1985-06-05

Substantially Equivalent

Victoreen, Inc.

FDA 510(k) clearance K851812 for DIGITAL SUBTRACTION ANTIOGRAPHY PHANTOM 76-700/711, Substantially Equivalent on 1985-06-05. Applicant: Victoreen, Inc.. Device class: 1.

Clearance details

Applicant: Victoreen, Inc.
Product code: Code IXF
Device class: Class 1
Regulation: 21 CFR 892.1940
Advisory panel: Radiology
Date received: 1985-04-26
Decision date: 1985-06-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carle Place, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXF

view all

K865100 — TISSUE-EQUIVALENT BREAST SIMULATOR1987-01-12
K834481 — DOPPLER PHANTOM FLOW CONTROL SYS1984-01-25
K834482 — TISSUE MIMICKING ULTRASOUND PHANTOMS1984-01-25
K810254 — 1.5` FOCAL SPOT RESOLUTION PATTERN1981-02-19

More clearances from Victoreen, Inc.

view all

K982937 — MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBER1998-11-19
K974112 — VACUDAP, MODEL 2000, 20011998-01-29
K973960 — MODEL 37-1851998-01-14
K964952 — VERIDOSE V (FIVE), MODEL NUMBER 37-7051997-07-21
K964785 — VERIDOSE DIODES1997-06-13

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