TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT— 510(k) K891180

Name: FDA 510(k) clearance K891180
Creator: U.S. Food and Drug Administration
Published: 1989-06-15

Substantially Equivalent

Ingress Technologies, Inc.

FDA 510(k) clearance K891180 for TRANSESOPHAGEAL ULTRASOUND ACCESSORIES KIT, Substantially Equivalent on 1989-06-15. Applicant: Ingress Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Ingress Technologies, Inc.
Product code: Code DXP
Device class: Class 2
Regulation: 21 CFR 870.2890
Advisory panel: Cardiovascular
Date received: 1989-03-06
Decision date: 1989-06-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DXP

view all

K812639 — UNICUFF1981-10-02

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