510(k) K801352

Device
Hemorrhoidal Ligation Instr. System
Applicant
DEPUY, INC.
510(k) number
K801352
Product code
FHN
Decision
Substantially Equivalent (SESE)
Decision date
1980-07-08
Date received
1980-06-09
Regulation
876.4400
Classification name
Ligator, Hemorrhoidal
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
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

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