BSNClass II
Filter, Conduction, Anesthetic
21 CFR 868.5130 / Anesthesiology
BSN is the FDA product code for Filter, Conduction, Anesthetic, a class II device type, regulated under 21 CFR 868.5130. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and one recall.
Classification record
- Product code
- BSN
- Device name
- Filter, Conduction, Anesthetic
- Regulation
- 21 CFR 868.5130
- Device class
- Class II
- Review panel
- Anesthesiology
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- Yes
- Ingested clearances
- 9
- Ingested recalls
- 1
Clearances, product code BSN
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1978 | 1 |
| 1991 | 1 |
| 1997 | 2 |
| 2002 | 1 |
| 2003 | 1 |
| 2009 | 1 |
| 2014 | 1 |
| 2019 | 1 |
Applicants with the most clearances
Product code BSN| Applicant | Clearances |
|---|---|
| EMD Millipore Corporation | 3 |
| Arbor Technologies, Inc. | 2 |
| Jelco Laboratories | 1 |
| Merck Millipore Ltd. | 1 |
| Pajunk GmbH Medizintechnologie | 1 |
| Abbott Medical | 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.
