Meddrains
by Armm Inc.
510(k) K931607
Meddrains is a Class I device made by Armm Inc., cleared under FDA 510(k) K931607 on 6 Aug 1993, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK931607 | Date6 Aug 1993 | StatusActive |
Official records
- FDA 510(k) database K931607
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- GBN
- FDA applicant
- Armm, Inc.
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4200
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K931607
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| MedDrain 25276C | 25276C | 10850082007988 | — | On the market |
| MedDrain 25277 | 25277 | 10850082007933 | — | On the market |
| MedDrain 25278 | 25278 | 10850082007971 | — | On the market |
| MedDrain 25287 | 25287 | 10850082007957 | — | On the market |
| MedDrain 25288 | 25288 | 10850082007865 | — | On the market |
| MedDrain 25288C | 25288C | 10850082007872 | — | On the market |
| MedDrain 25289C | 25289C | 10850005416064 | — | On the market |
| MedDrain 25296 | 25296 | 10850005416057 | — | On the market |
| MedDrain 25297 | 25297 | 10850082007940 | — | On the market |
| MedDrain 25298 | 25298 | 10850005416026 | — | On the market |