510(k) K003873

Device
MENTOR SELF-CATH CLOSED SYSTEM
Applicant
Mentor Corp.
510(k) number
K003873
Product code
FCM
Decision
Substantially Equivalent (SESE)
Decision date
2001-03-29
Date received
2000-12-15
Regulation
876.5130
Classification name
Tray, Catheterization, Sterile Urethral, With Or Without Catheter (Kit)
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
DONNA A CRAWFORD
Address
201 Mentor Dr. Santa Barbara CA US 93111 93111

FDA Registration Numbers

Source Documents

510(k) summary PDF

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