Celluma POD C/US
Celluma POD C/US (CPOD-001) is a Class II device made by BioPhotas, Inc., cleared under FDA 510(k) K171323 on 1 Sep 2017 and listed in FDA GUDID since 11 Jun 2020 (UDI-DI 00850523007501), 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 | GUDID listing | Number00850523007501 | Date11 Jun 2020 | StatusListed |
| United States | FDA 510(k) | NumberK171323 | Date1 Sep 2017 | StatusActive |
Official records
- AccessGUDID record 00850523007501
- FDA 510(k) database K171323
Across registries
- FDA 510(k) K171323 decided 1 Sep 2017 Active
- FDA GUDID UDI-DI 00850523007501 listed 11 Jun 2020 Listed
Timeline
- Cleared FDA 510(k) K171323
- Listed FDA GUDID 00850523007501
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Celluma
- Generic name
- Blue/red/infrared phototherapy lamp
- Model / Ref / Catalog
- POD C/US, CPOD-001
- Primary DI / UDI-DI
- 00850523007501
- 510(k) Number
- FDA product code
- OLP, OHS, ILY
- GMDN term
- Blue/red/infrared phototherapy lamp
- Device class
- Class II
- Regulation number
- 878.4810, 890.5500
- GUDID distribution status
- In Commercial Distribution
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