Cannula Faceplate 310603
by Boston Medical Products, Inc. 2 variants
Cannula Faceplate 310603 is a Class II device made by Boston Medical Products, Inc., cleared under FDA 510(k) K802916 on 19 Dec 1980 and listed in FDA GUDID since 29 Sep 2022 (UDI-DI 14063107100052), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number14063107100052 | Date29 Sep 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK802916 | Date19 Dec 1980 | StatusActive |
Official records
- AccessGUDID record 14063107100052
- FDA 510(k) database K802916
Across registries
- FDA 510(k) K802916 decided 19 Dec 1980 Active
- FDA GUDID UDI-DI 14063107100052 listed 29 Sep 2022 Listed
Timeline
- Cleared FDA 510(k) K802916
- Listed FDA GUDID 14063107100052
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Cannula Faceplate
- Generic name
- Tracheostomy tube dressing
- Model / Ref / Catalog
- 310603
- Primary DI / UDI-DI
- 14063107100052
- 510(k) Number
- FDA product code
- BTO
- GMDN term
- Tracheostomy tube dressing
- Device class
- Class II
- Regulation number
- 868.5800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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