Lyophilized Platelets 5356
Lyophilized Platelets 5356 is a Class II device made by Helena Laboratories, Corp., cleared under FDA 510(k) K840329 on 5 Apr 1984 and listed in FDA GUDID since 7 Sep 2016 (UDI-DI M52553560), 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 | NumberM52553560 | Date7 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK840329 | Date5 Apr 1984 | StatusActive |
Official records
- FDA 510(k) database K840329
Across registries
- FDA 510(k) K840329 decided 5 Apr 1984 Active
- FDA GUDID UDI-DI M52553560 listed 7 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K840329
- Listed FDA GUDID M52553560
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lyophilized Platelets
- Generic name
- von Willebrand factor: ristocetin cofactor complex activity (vWF:RCO) IVD, reagent
- Model / reference
- 5356
- Primary DI / UDI-DI
- M52553560
- 510(k) Number
- FDA product code
- GGP
- GMDN term
- von Willebrand factor: ristocetin cofactor complex activity (vWF:RCO) IVD, reagent
- Device class
- Class II
- Regulation number
- 864.7290
- GUDID distribution status
- In Commercial Distribution
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