Curafil Wound Gel Dressing
K943073 is the FDA 510(k) clearance record for CURAFIL WOUND GEL DRESSING, cleared for Kendall Healthcare Products Co. Div.Of Tyco Health on under FDA product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic). FDA records list 66 510(k) clearances for Kendall Healthcare Products Co. Div.Of Tyco Health, from to . As of , FDA records show no recalls naming K943073.
Clearance record
- Decision date
- Received
- (28 days to decision)
- Product code
- MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
- Device class
- Unclassified
- Review panel
- Unknown
- Applicant
- Kendall Healthcare Products Co. Div.Of Tyco Health 15 Hampshire St., Mansfield MA
- Third party review
- No
Clearances, product code MGQ
Trailing 12 monthsFDA records hold no clearances under product code MGQ in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
