MULTI-AD FLUID DISPENSING PUMP MP-3000— 510(k) K801008

Name: FDA 510(k) clearance K801008
Creator: U.S. Food and Drug Administration
Published: 1980-06-02

Substantially Equivalent

Burron Medical Products, Inc.

FDA 510(k) clearance K801008 for MULTI-AD FLUID DISPENSING PUMP MP-3000, Substantially Equivalent on 1980-06-02. Applicant: Burron Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Burron Medical Products, Inc.
Product code: Code KYX
Device class: Class 1
Regulation: 21 CFR 880.6430
Advisory panel: General Hospital
Date received: 1980-04-28
Decision date: 1980-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KYX

view all

K143177 — KleenGel Dispenser2015-09-14
K980109 — CYCLOTECH CYCLOSPORINE ORAL SOLUTIONS DISPENSER1998-08-18
K954181 — CANYONS BI-DIRECTIONAL CHECK VALVE1995-11-29
K830571 — BOTTLE ADAPTER1983-03-24
K800362 — FLUID DISPENSING SYSTEM1980-03-12

More clearances from Burron Medical Products, Inc.

view all

K870403 — CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE1987-05-01
K862412 — INTESTOPLANT1986-11-13
K861479 — CAVAFIX, CENTRAL VENOUS CATHETER KIT1986-07-01
K860126 — STIMUPLEX, NERVE STIMULATOR1986-02-28
K851293 — IMPLANTOFIX1986-01-09

Adverse events under product code KYX

product code KYX

Death: 3
Other: 8
Total: 11

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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