DQRClass II
Cannula, Catheter
21 CFR 870.1300 / Cardiovascular
DQR is the FDA product code for Cannula, Catheter, a class II device type, regulated under 21 CFR 870.1300. As of , FDA records hold 25 510(k) clearances under this code, the most recent dated , and 26 recalls.
Classification record
- Product code
- DQR
- Device name
- Cannula, Catheter
- Regulation
- 21 CFR 870.1300
- 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
- 25
- Ingested recalls
- 26
Clearances, product code DQR
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1977 | 1 |
| 1978 | 1 |
| 1980 | 1 |
| 1981 | 1 |
| 1982 | 1 |
| 1987 | 3 |
| 1988 | 5 |
| 1989 | 5 |
| 1990 | 1 |
| 1991 | 1 |
| 1996 | 1 |
| 2003 | 1 |
| 2005 | 1 |
| 2008 | 1 |
| 2013 | 1 |
Applicants with the most clearances
Product code DQR| Applicant | Clearances |
|---|---|
| Shiley, Inc. | 3 |
| Harbor Medical Devices, Inc. | 2 |
| Medsurg Industries, Inc. | 2 |
| Research Medical, Inc. | 2 |
| Boston Scientific Corporation | 1 |
| Argon Medical Corp. | 1 |
| Bentley Laboratories, Inc. | 1 |
| Cardiacassist, Inc. | 1 |
| Daig Corp. | 1 |
| Datascope Corp. | 1 |
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.