DeVilbiss 3655LTPL-EME
DeVilbiss 3655LTPL-EME 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 21 Apr 2017 (UDI-DI 00885304001256), active (FDA 510(k)), not in commercial distribution (GUDID) 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 | Number00885304001256 | Date21 Apr 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020932 | Date28 Jun 2002 | StatusActive |
Official records
- AccessGUDID record 00885304001256
- FDA 510(k) database K020932
Across registries
- FDA 510(k) K020932 decided 28 Jun 2002 Active
- FDA GUDID UDI-DI 00885304001256 listed 21 Apr 2017 Listed
Timeline
- Cleared FDA 510(k) K020932
- Listed FDA GUDID 00885304001256
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- Withdrawn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
- 3655LTPL-EME
- Primary DI / UDI-DI
- 00885304001256
- 510(k) Number
- FDA product code
- CAF
- GMDN term
- Medical device air compressor
- Device class
- Class II
- Regulation number
- 868.5630
- GUDID distribution status
- Not in Commercial Distribution
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