Conveen(R) Leg BAG(500 ML)

FDA 510(k) K924406 · Coloplast A/S

Substantially Equivalent

510(k) numberK924406

Submission

Device name
Conveen(R) Leg BAG(500 ML)
Applicant
Coloplast A/S
Fort Woth, TX, US
Received
August 25, 1992
Decision date
October 30, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FAQ – Bag, Urine Collection, Leg, For External Use, Sterile
Device class
Class I (low risk)
Regulation
21 CFR 876.5250
Specialty
Gastroenterology, Urology

Other 510(k)s with product code FAQ

510(k)DeviceApplicantDecision
K962604Prosys Custom Fit Leg Bag with Preattached Adjustable Inlet Tube for Patient SizingFAQ · Traditional Convatec, A Division of E.R. Squibb & Sons07/18/1996SE
K960217CPR Urine BagFAQ · Traditional Custom Pack Reliability03/28/1996SE
K955609Conveen Urine Bag - SterileFAQ · Traditional Coloplast Corp.12/29/1995SE
K953767Prosys Bedside Drainage BagFAQ · Traditional Convatec, A Division of E.R. Squibb & Sons12/20/1995SE
K953783Conveen Leg Bag StrapFAQ · Traditional Coloplast Corp.09/13/1995SE
K951945Prosys Leg BagFAQ · Traditional Convatec, A Division of E.R. Squibb & Sons05/25/1995SE
K945204Urine Collector & AccessoriesFAQ · Traditional Nelmed Corp.11/02/1994SE
K934052Alpine Reusable Leg BagsFAQ · Traditional Sierra Laboratories, Inc.01/07/1994SE
K931727Urinary Drainage Bag CaddyFAQ · Traditional Neotech Products, Inc.07/23/1993SE
K926035Bard Leg Bag HolderFAQ · Traditional C.R. Bard, Inc.12/17/1992SE

More from C.R. Bard, Inc.

510(k)DeviceDecision
K262045Luja SoftEZD · Special 07/07/2026SE
K221874Altis Single Incision Sling SystemPAH · Special 02/15/2023SE
K220420Saffron Fixation SystemPBQ · Traditional 06/10/2022SE
K191536Biatain Silicone AgFRO · Traditional 02/21/2020SE
K181811ReTrace Ureteral Access SheathFED · Special 09/07/2018SE
K173527Digitex Delivery DevicePWI · Traditional 02/12/2018SE
K140310Peristeen Anal Irrigation SystemKNT · Traditional 09/03/2015SE
K150935SpeediCath Compact EveGBM · Traditional 07/02/2015SE
K150927Orchestra Hydrophilic Guidewire standard angled, Orchestra Hydrophilic Guidewire…OCY · Traditional 05/27/2015SE
K143182Speedicath Compact MaleGBM · Traditional 01/20/2015SE

Questions and answers

When was Conveen(R) Leg BAG(500 ML) cleared by the FDA?

Conveen(R) Leg BAG(500 ML) (K924406) received a 510(k) decision of Substantially Equivalent on October 30, 1992, 66 days after the submission was received.

What is the product code of K924406?

The FDA product code is FAQ – Bag, Urine Collection, Leg, For External Use, Sterile, a Class I (low risk) device regulated under 21 CFR 876.5250.