P-1 ULTRASONIC ARTERIOGRAPH— 510(k) K761288

Substantially Equivalent

D. Eugene Hokanson

FDA 510(k) clearance K761288 for P-1 ULTRASONIC ARTERIOGRAPH, Substantially Equivalent on 1976-12-28. Applicant: D. Eugene Hokanson. Device class: 2.

Clearance details

Applicant
D. Eugene Hokanson
Product code
Code DPW
Device class
Class 2
Regulation
21 CFR 870.2100
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Mchenry, IL, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DPW

view all

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