FDA.reportPublic FDA data

510(k) K802430

Device
NEBULIZER, MEDICINAL
Applicant
DHD MEDICAL PRODUCTS DIV. DIEMOLDING CORP.
510(k) number
K802430
Product code
EPN  
Decision
Substantially Equivalent (SESE)
Decision date
1980-10-23
Date received
1980-10-06
Regulation
874.5220
Classification name
Pump, Nebulizer, Manual
Medical specialty
Ear Nose & Throat
Review panel
Ear Nose & Throat
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code EPN  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K896090DEVILBISS MODEL 6300DDevilbiss Health Care, Inc.1989-11-30

Legacy Summary#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases

FDA Review#

Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases