The MMG 5 in 1 Connector
FDA 510(k) K863912 · Medical Marketing Group
510(k) numberK863912
Submission
- Device name
- The MMG 5 in 1 Connector
- Applicant
- Medical Marketing Group
Decatur, GA, US - Received
- October 8, 1986
- Decision date
- October 27, 1986
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- BYX – Tubing, Pressure And Accessories
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 868.5860
- Specialty
- Anesthesiology
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| K935835 | Busse Plastic Tubing Connectors and AccessoriesBYX · Traditional | Busse Hospital Disposables, Inc. | 01/12/1994SE |
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| K913422 | Oxygen Tubing, 81503BYX · Traditional | Specialty Packaging Producs, Inc. | 01/30/1992SE |
| K914980 | Hex, Quad, or Rail Block Manifold AccessoriesBYX · Traditional | Medical Fittings, Inc. | 01/21/1992SE |
| K912763 | Ohmeda Style Check Units (Female Couplers)BYX · Traditional | Medical Fittings, Inc. | 10/15/1991SE |
| K905091 | Various Male Quick Connects.BYX · Traditional | Medical Fittings, Inc. | 03/04/1991SE |
More from Medical Fittings, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K910022 | Mmg/O'Neil Urinary Catheterization System KitFCM · Traditional | 04/02/1991SEKD |
| K884819 | O'Neil Urinary Catheter IntroducerKNY · Traditional | 02/17/1989SE |
| K874682 | MMG Catheter Plug W/Drainage Tube CoverKOD · Traditional | 01/27/1988SE |
| K871999 | MMG Uro-Self CatheterGBM · Traditional | 08/25/1987SE |
| K840838 | MMG Connective TubingGAZ · Traditional | 03/30/1984SE |
| K821168 | Disposable Urinary Legbag W/StrapKNX · Traditional | 05/24/1982SE |
| K811469 | MMG Urinary Drainage TubingKNX · Traditional | 06/12/1981SE |
| K800694 | MMG Disposable Urinary Leg BagKNX · Traditional | 05/30/1980SE |
| K791847 | Aspri-LukeBYZ · Traditional | 10/02/1979SE |
| K790279 | Catheter, MMG Latex ExternalKNX · Traditional | 03/06/1979SE |
Questions and answers
When was The MMG 5 in 1 Connector cleared by the FDA?
The MMG 5 in 1 Connector (K863912) received a 510(k) decision of Substantially Equivalent on October 27, 1986, 19 days after the submission was received.
What is the product code of K863912?
The FDA product code is BYX – Tubing, Pressure And Accessories, a Class I (low risk) device regulated under 21 CFR 868.5860.