MMKClass II
Container, Sharps
21 CFR 880.5570 / General Hospital
MMK is the FDA product code for Container, Sharps, a class II device type, regulated under 21 CFR 880.5570. As of , FDA records hold 114 510(k) clearances under this code, the most recent dated , and 3 recalls.
Classification record
- Product code
- MMK
- Device name
- Container, Sharps
- Regulation
- 21 CFR 880.5570
- Device class
- Class II
- Review panel
- General Hospital
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 114
- Ingested recalls
- 3
Clearances, product code MMK
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 2 |
| 1978 | 1 |
| 1979 | 4 |
| 1980 | 1 |
| 1981 | 3 |
| 1982 | 1 |
| 1983 | 2 |
| 1984 | 1 |
| 1986 | 4 |
| 1987 | 1 |
| 1988 | 1 |
| 1989 | 2 |
| 1990 | 3 |
| 1991 | 4 |
| 1992 | 3 |
| 1994 | 7 |
| 1995 | 7 |
| 1996 | 2 |
| 1997 | 2 |
| 1998 | 3 |
| 1999 | 1 |
| 2000 | 1 |
| 2002 | 2 |
| 2006 | 1 |
| 2007 | 4 |
| 2008 | 6 |
| 2009 | 4 |
| 2010 | 1 |
| 2011 | 1 |
| 2012 | 2 |
| 2013 | 5 |
| 2014 | 6 |
| 2015 | 3 |
| 2016 | 4 |
| 2017 | 1 |
| 2018 | 1 |
| 2019 | 4 |
| 2020 | 1 |
| 2021 | 3 |
| 2022 | 1 |
| 2023 | 3 |
| 2025 | 3 |
| 2026 | 2 |
Applicants with the most clearances
Product code MMK| Applicant | Clearances |
|---|---|
| Bemis Mfg. Co. | 7 |
| Sage Products LLC | 5 |
| Anago, Inc. | 4 |
| Ningbo Maxcon Medical Technology Co., Ltd | 4 |
| Oak Ridge Products | 3 |
| Pureway Compliance, Inc. | 3 |
| Richard-Allan Medical Ind., Inc. | 3 |
| Biosystems S.A. | 2 |
| Daniels Corporation Pty, Inc. | 2 |
| Devon Industries, Inc. | 2 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.