Medline Premium Leg Bag, Medline Fabric Bac Leg Bag, Medline Urinary Leg Bag
FDA 510(k) K972887 · Medline Industries, Inc.
510(k) numberK972887
Submission
- Device name
- Medline Premium Leg Bag, Medline Fabric Bac Leg Bag, Medline Urinary Leg Bag
- Applicant
- Medline Industries, Inc.
Mundelein, IL, US - Received
- August 5, 1997
- Decision date
- December 11, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KNX – Collector, Urine, (And Accessories) For Indwelling Catheter
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.5250
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code KNX
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|---|---|---|---|
| K110518 | IbagKNX · Traditional | Future Path Medical, LLC | 06/24/2011SE |
| K973364 | 4L Drainage Bag, 4L Bag for Peritoneal Dialysis, 4L Urinary Drainage BagKNX · Traditional | Maersk Medical A/S | 03/17/1998SE |
| K971271 | Besecure External Urinary Collection SystemKNX · Traditional | Urology Research Intl., Inc. | 08/18/1997SE |
| K971929 | Amsino Urinary Leg BagKNX · Traditional | Amsino Intl., Inc. | 08/06/1997SE |
| K971764 | Welcon Hue-Vu Urinary Drainage BagKNX · Traditional | Welcon, Inc. | 07/29/1997SE |
| K964690 | Liberty ValveKNX · Traditional | Cleveland Medical Devices, Inc. | 03/21/1997SE |
| K964745 | Amsino Urinary Drainage BagKNX · Traditional | Amsino Intl., Inc. | 03/18/1997SE |
| K962652 | Urinary Drainage Bag, (Reorder No. 0749 - Product No. 900-749)KNX · Traditional | Customed, Inc. | 10/04/1996SE |
| K960949 | Prosys Bedside Drainage Bag (Sterile) Model 650167KNX · Traditional | Bristol-Myers Squibb | 04/19/1996SE |
| K952208 | Prosys Leg BagKNX · Traditional | Convatec, A Division of E.R. Squibb & Sons | 08/15/1995SE |
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Questions and answers
When was Medline Premium Leg Bag, Medline Fabric Bac Leg Bag, Medline Urinary Leg Bag cleared by the FDA?
Medline Premium Leg Bag, Medline Fabric Bac Leg Bag, Medline Urinary Leg Bag (K972887) received a 510(k) decision of Substantially Equivalent on December 11, 1997, 128 days after the submission was received.
What is the product code of K972887?
The FDA product code is KNX – Collector, Urine, (And Accessories) For Indwelling Catheter, a Class II (moderate risk) device regulated under 21 CFR 876.5250.