CCWClass I
Laryngoscope, Rigid
21 CFR 868.5540 / Anesthesiology
CCW is the FDA product code for Laryngoscope, Rigid, a class I device type, regulated under 21 CFR 868.5540. As of , FDA records hold 64 510(k) clearances under this code, the most recent dated , and 53 recalls.
Classification record
- Product code
- CCW
- Device name
- Laryngoscope, Rigid
- Regulation
- 21 CFR 868.5540
- Device class
- Class I
- Review panel
- Anesthesiology
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 64
- Ingested recalls
- 53
Clearances, product code CCW
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1983 | 6 |
| 1984 | 1 |
| 1985 | 2 |
| 1986 | 1 |
| 1987 | 1 |
| 1988 | 8 |
| 1989 | 1 |
| 1990 | 3 |
| 1991 | 3 |
| 1992 | 5 |
| 1993 | 5 |
| 1994 | 5 |
| 1995 | 6 |
| 1996 | 3 |
| 1997 | 2 |
| 1998 | 1 |
| 1999 | 1 |
| 2004 | 1 |
| 2006 | 3 |
| 2007 | 1 |
| 2012 | 1 |
| 2014 | 1 |
| 2017 | 1 |
| 2019 | 1 |
Applicants with the most clearances
Product code CCW| Applicant | Clearances |
|---|---|
| Augustine Medical, Inc. | 5 |
| Eastmed Enterprises, Inc. | 5 |
| Minrad, Inc. | 3 |
| Michael S. Upsher | 2 |
| Wilson Greatbatch Technologies, Inc. | 2 |
| Achi Corp. | 1 |
| Acorn Group, Inc. | 1 |
| Arco Medic, Ltd. | 1 |
| Armstrong Ind., Inc. | 1 |
| Avulunga Pty., Ltd. | 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.