510(k) K873177

Device
Devine (suprapubic Sound And Guide)
Applicant
PENN MEDICAL DEVICES, INC.
510(k) number
K873177
Product code
KOE
Decision
Substantially Equivalent (SESE)
Decision date
1987-10-14
Date received
1987-08-12
Regulation
876.5520
Classification name
Dilator, Urethral
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
CHARLES E MEISCH
Address
12 Ridge St. Basking Ridge NJ US 07920 07920

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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