OLYMPUS ANGIOSCOPY PUMP— 510(k) K871422

Substantially Equivalent

Olympus Corp.

FDA 510(k) clearance K871422 for OLYMPUS ANGIOSCOPY PUMP, Substantially Equivalent on 1987-08-12. Applicant: Olympus Corp.. Device class: 2.

Clearance details

Applicant
Olympus Corp.
Product code
Code DQI
Device class
Class 2
Regulation
21 CFR 870.1800
Advisory panel
Cardiovascular
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Lake Success, NY, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code DQI

view all

More clearances from Olympus Corp.

view all

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