MULTI-AD FLUID DISPENSING SYSTEM— 510(k) K792227

Name: FDA 510(k) clearance K792227
Creator: U.S. Food and Drug Administration
Published: 1979-12-20

Substantially Equivalent

National Patent Development Corp.

FDA 510(k) clearance K792227 for MULTI-AD FLUID DISPENSING SYSTEM, Substantially Equivalent on 1979-12-20. Applicant: National Patent Development Corp.. Device class: 1.

Clearance details

Applicant: National Patent Development Corp.
Product code: Code KYX
Device class: Class 1
Regulation: 21 CFR 880.6430
Advisory panel: General Hospital
Date received: 1979-11-05
Decision date: 1979-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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
K801008 — MULTI-AD FLUID DISPENSING PUMP MP-30001980-06-02

More clearances from National Patent Development Corp.

view all

K843974 — VARIABLE TEMPERATURE CAUTERY DEVICE1985-02-26
K832699 — HYDRON WOUND DRESSING FAST SEAT KIT1984-04-27
K822793 — PIO ROOT CANAL INDICATOR1982-10-22
K820028 — ZEON COMPOSITE RESIN LIGHT CURE SYS1982-03-11
K820006 — ZEON COMPOSITE RESIN SYSTEM1982-01-22

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.