The Reel Thing (Modification)
FDA 510(k) K955439 · Biomedical Devices, Inc.
510(k) numberK955439
Submission
- Device name
- The Reel Thing (Modification)
- Applicant
- Biomedical Devices, Inc.
Irvine, CA, US - Received
- November 13, 1995
- Decision date
- December 26, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- GBX – Catheter, Irrigation
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4200
- Specialty
- General, Plastic Surgery
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|---|---|---|---|
| K131659 | Moerae Vein Preparation KitGBX · Traditional | Moerae Matrix, Inc. | 03/03/2014SE |
| K082725 | Graftguard Pressure Controlling SyringeGBX · Traditional | Maquet Cardiovascular, LLC | 12/17/2008SE |
| K052286 | Deutsch Anti-Blockage Wound DrainGBX · Traditional | The Catheter Exchange, Inc. | 10/21/2005SE |
| K043515 | GraftsaverGBX · Traditional | Vescare, Inc. | 03/31/2005SE |
| K013417 | Misonix Irrigation System Moedl BC20PGBX · Traditional | Misonix, Inc. | 01/10/2002SE |
| K000704 | DMC Saphenous Vein Distention System (SVDS)GBX · Traditional | Dmc Medical, Ltd. | 05/19/2000SE |
| K974233 | Lysonix Irrigation SystemGBX · Traditional | Lysonix, Inc. | 02/03/1998SE |
| K973703 | Jackson-Pratt Hemaduct Wound Drain, Jackson-Pratt Gold Hemaduct Wound DrainGBX · Traditional | Allegiance Healthcare Corp. | 12/04/1997SE |
| K972635 | Ultracell Suction SpongeGBX · Traditional | Ultracell Medical Technologies, Inc. | 10/01/1997SE |
| K965146 | Flat Closed Wound Drain with TrocarGBX · Traditional | Axiom Medical, Inc. | 03/10/1997SE |
More from Axiom Medical, Inc.
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|---|---|---|
| K931847 | Bio-Prep Cement RestrictorLZN · Traditional | 06/28/1994SE |
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| K925982 | BMD Air/Oxygen BlenderBZR · Traditional | 10/07/1993SE |
| K903533 | Steri-ShieldFXY · Traditional | 10/19/1990SE |
| K902677 | Steri-ShieldFXY · Traditional | 08/17/1990SE |
| K830605 | Pump Pall Ambulatory Insulin InfusionFRN · Traditional | 03/31/1983SE |
Questions and answers
When was The Reel Thing (Modification) cleared by the FDA?
The Reel Thing (Modification) (K955439) received a 510(k) decision of Substantially Equivalent on December 26, 1995, 43 days after the submission was received.
What is the product code of K955439?
The FDA product code is GBX – Catheter, Irrigation, a Class I (low risk) device regulated under 21 CFR 878.4200.