510(k) K771738

Device: MALE URINAL
Applicant: Bemis Health Care
510(k) number: K771738
Product code: FNP
Decision: Substantially Equivalent (SESE)
Decision date: 1977-09-28
Date received: 1977-09-15
Regulation: 880.6730
Classification name: Urinal
Medical specialty: General Hospital
Review panel: General Hospital
Device class: 1
Clearance type: Traditional
Third party reviewed: N

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