Atlas FDA

MENTOR SELF-CATH CLOSED SYSTEM

FDA 510(k) clearance K003873 · decided 2001-03-29

Clearance details

K-number
K003873
Device name
MENTOR SELF-CATH CLOSED SYSTEM
Applicant
Mentor Corp.
Decision
Substantially Equivalent
Date received
2000-12-15
Decision date
2001-03-29
Days to decision
104 days
Clearance type
Traditional
Product code
FCM
Device class
2
Regulation number
876.5130
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Santa Barbara, CA, US
Third-party review
No
Expedited review
No

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AMSELF CLOSED CATHETERIZATION SYSTEM (K082831)Amsino International, Inc.2008-10-23
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AMSURE URETHRAL CATHETERIZATION TRAY (K030712)Amsino International, Inc.2003-05-23
AMSURE FOLEY INSERTION TRAY (K030664)Amsino International, Inc.2003-05-23
THE O'NEIL STERILE FIELD URINARY CATHETER KIT WITH PREP PADS (K011055)Go Medical Industries Pty. , Ltd.2001-06-06
RUSCH MMG/O'NEIL CATHETER (K010420)Rusch, Inc.2001-05-09
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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MENTOR™ MemoryGel™ Silicone Gel-Filled Breast Implants (P030053/S084)Mentor Corp.2025-12-17
MemoryGel™ Silicone Gel-Filled Breast Implants (P030053/S080)Mentor Corp.2025-08-12
MENTOR™ MemoryGel™ Silicone Gel-Filled Breast Implants (P030053/S082)Mentor Corp.2025-08-08
Mentor MemoryGel® Breast Implants (P030053/S072)Mentor Corp.2025-08-06
MENTOR MemoryGel Enhance Breast Implants (P030053/S077)Mentor Corp.2025-07-03
MENTOR™ MemoryGel™ Enhance Breast Implants (P030053/S081)Mentor Corp.2025-06-18
MEMORYGEL SILICONE GEL -FILLED BREAST IMPLANTS (P030053/S079)Mentor Corp.2025-05-21
MENTOR™ MemoryGel™ Enhance Breast Implants (P030053/S078)Mentor Corp.2025-02-14