DQDClass II
Stethoscope, Electronic
21 CFR 870.1875 / Cardiovascular
DQD is the FDA product code for Stethoscope, Electronic, a class II device type, regulated under 21 CFR 870.1875. As of , FDA records hold 156 510(k) clearances under this code, the most recent dated , and no recalls.
Classification record
- Product code
- DQD
- Device name
- Stethoscope, Electronic
- Regulation
- 21 CFR 870.1875
- Device class
- Class II
- Review panel
- Cardiovascular
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 156
- Ingested recalls
- 0
Clearances, product code DQD
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 6 |
| 1978 | 2 |
| 1979 | 5 |
| 1980 | 2 |
| 1981 | 1 |
| 1983 | 1 |
| 1984 | 1 |
| 1985 | 2 |
| 1986 | 3 |
| 1987 | 2 |
| 1988 | 2 |
| 1989 | 1 |
| 1990 | 1 |
| 1992 | 1 |
| 1994 | 1 |
| 1995 | 4 |
| 1996 | 4 |
| 1997 | 3 |
| 1999 | 4 |
| 2000 | 5 |
| 2001 | 5 |
| 2002 | 4 |
| 2003 | 4 |
| 2004 | 4 |
| 2005 | 6 |
| 2006 | 4 |
| 2007 | 2 |
| 2008 | 1 |
| 2009 | 6 |
| 2010 | 1 |
| 2011 | 4 |
| 2012 | 2 |
| 2013 | 5 |
| 2015 | 2 |
| 2016 | 3 |
| 2017 | 4 |
| 2018 | 4 |
| 2019 | 4 |
| 2020 | 6 |
| 2021 | 4 |
| 2022 | 8 |
| 2023 | 10 |
| 2024 | 4 |
| 2025 | 3 |
| 2026 | 5 |
Applicants with the most clearances
Product code DQD| Applicant | Clearances |
|---|---|
| Rnk Products, Inc. | 6 |
| 3M Company | 5 |
| Chip Ideas Electronics S.L. | 5 |
| Eko Devices, Inc. | 5 |
| Zargis Medical Corp. | 5 |
| Amdia Medical Products | 4 |
| Andromed, Inc. | 4 |
| Sparrow Acoustics Inc. | 4 |
| Swartz Medical Equipment | 4 |
| American Diagnostic Corp. | 3 |
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.