C3 External Male Bladder Control Device

FDA 510(k) K974040 · Timm Research Co.

Substantially Equivalent

510(k) numberK974040

Submission

Device name
C3 External Male Bladder Control Device
Applicant
Timm Research Co.
Eden Prairie, MN, US
Received
October 24, 1997
Decision date
July 14, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FHA – Clamp, Penile
Device class
Class I (low risk)
Regulation
21 CFR 876.5160
Specialty
Gastroenterology, Urology

Other 510(k)s with product code FHA

510(k)DeviceApplicantDecision
K971992Uromed Alternative Bladder Control Continence DEVICE(ABCPN-0026)FHA · Traditional Uromed Corp.08/01/1997SE
K970308Mentor Urology Triple Rib Occlusion Wrap for Male IncontinenceFHA · Traditional Mentor Urology, Inc.04/02/1997SE
K964580Cap-Aid (Improved)FHA · Traditional Nebel, Inc.01/10/1997SE
K955810U-TexFHA · Traditional Laborie Medical Technologies, Ltd.01/24/1996SE
K954959Cap-AidFHA · Traditional Nebl, Inc.12/06/1995SE
K952841The AssistantFHA · Traditional Apple Medical Corp.08/18/1995SE
K896160Williams Penile Anesthetic RetainerFHA · Traditional Cook Urological, Inc.02/16/1990SE
K885323Dacomed External Male Continence DeviceFHA · Traditional Dacomed Corp.02/08/1989SE
K863227Cook-Vpi Continence CuffFHA · Traditional Cook Urological, Inc.02/03/1987SE
K780137Clamp, Incontinence, BaumruckerFHA · Traditional Greenwald Surgical Co., Inc.04/28/1978SE

Questions and answers

When was C3 External Male Bladder Control Device cleared by the FDA?

C3 External Male Bladder Control Device (K974040) received a 510(k) decision of Substantially Equivalent on July 14, 1998, 263 days after the submission was received.

What is the product code of K974040?

The FDA product code is FHA – Clamp, Penile, a Class I (low risk) device regulated under 21 CFR 876.5160.