K133443Substantially Equivalent
Marathon No Sting Liquid Skin Protectant
Advanced Medical Solutions (Plymouth), Ltd., Plympton, Plymouth, Devon, GB / Traditional, Substantially Equivalent
K133443 is the FDA 510(k) clearance record for MARATHON NO STING LIQUID SKIN PROTECTANT, a class I device, cleared for Advanced Medical Solutions (Plymouth), Ltd. on under FDA product code KMF (Bandage, Liquid). FDA records list 5 510(k) clearances for Advanced Medical Solutions (Plymouth), Ltd., from to . As of , FDA records show no recalls naming K133443.
Clearance record
- Decision date
- Received
- (240 days to decision)
- Product code
- KMF Bandage, Liquid
- Regulation
- 21 CFR 880.5090
- Device class
- Class I
- Review panel
- General Hospital
- Applicant
- Advanced Medical Solutions (Plymouth), Ltd. Western Wood Way, Langage Science Park, Plympton, Plymouth, Devon, GB
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code KMF
Trailing 12 monthsFDA records hold no clearances under product code KMF 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.
