Cellusheet, Cellufil
510(k) K213092
Cellusheet, Cellufil is a device classified as Unclassified made by Human Biosciences Inc., cleared under FDA 510(k) K213092 on 15 Dec 2021, active as of 8 Nov 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 | NumberK213092 | Date15 Dec 2021 | StatusActive |
Official records
- FDA 510(k) database K213092
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KGN
- FDA applicant
- Human Biosciences, Inc.
- Device class
- U
- Advisory committee
- Unknown
- FDA decision
- SESE Substantially Equivalent
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