DeVilbiss 3655LT
DeVilbiss 3655LT is a Class II device made by DeVilbiss Healthcare LLC., cleared under FDA 510(k) K020932 on 28 Jun 2002 and listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00885304001782), 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 | Number00885304001782 | Date23 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020932 | Date28 Jun 2002 | StatusActive |
Official records
- AccessGUDID record 00885304001782
- FDA 510(k) database K020932
Across registries
- FDA 510(k) K020932 decided 28 Jun 2002 Active
- FDA GUDID UDI-DI 00885304001782 listed 23 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K020932
- Listed FDA GUDID 00885304001782
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- DeVilbiss
- Generic name
- Medical device air compressor
- Model / Ref / Catalog
- 3655LT
- Primary DI / UDI-DI
- 00885304001782
- 510(k) Number
- FDA product code
- CAF, BTI
- GMDN term
- Medical device air compressor
- Device class
- Class II
- Regulation number
- 868.5630, 868.6250
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Medical device air compressor.