MGQUnclassified
Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Unknown
MGQ is the FDA product code for Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic. As of , FDA records hold 145 510(k) clearances under this code, the most recent dated , and 14 recalls.
Classification record
- Product code
- MGQ
- Device name
- Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 145
- Ingested recalls
- 14
Clearances, product code MGQ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1991 | 2 |
| 1992 | 8 |
| 1993 | 7 |
| 1994 | 17 |
| 1995 | 23 |
| 1996 | 20 |
| 1997 | 13 |
| 1998 | 16 |
| 1999 | 16 |
| 2000 | 6 |
| 2001 | 4 |
| 2002 | 4 |
| 2003 | 3 |
| 2004 | 3 |
| 2005 | 1 |
| 2009 | 1 |
| 2017 | 1 |
Applicants with the most clearances
Product code MGQ| Applicant | Clearances |
|---|---|
| Fidia Pharmaceutical Corp. | 10 |
| Brennen Medical, Inc. | 7 |
| Carrington Laboratories, Inc. | 7 |
| MEDLINE INDUSTRIES, LP - Northfield | 5 |
| MPM Medical | 5 |
| Procyte Corp. | 5 |
| Derma Sciences, Inc. | 4 |
| Renaissance Medical, Inc. | 4 |
| Renaissance Pharmaceutical, Inc. | 4 |
| Acrymed, Inc. | 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.
