Amy AY7932
Amy AY7932 is a Class II device made by Randox Laboratories, Ltd., cleared under FDA 510(k) K953211 on 21 Jun 1996 and listed in FDA GUDID since 9 Sep 2016 (UDI-DI 05055273200652), active as of 22 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05055273200652 | Date9 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK953211 | Date21 Jun 1996 | StatusActive |
Official records
- AccessGUDID record 05055273200652
- FDA 510(k) database K953211
Across registries
- FDA 510(k) K953211 decided 21 Jun 1996 Active
- FDA GUDID UDI-DI 05055273200652 listed 9 Sep 2016 Listed
Recalls
-
- Terminated Z-2923-2020
Amylase AY3805 batch 480449 and Pancreatic Amylase AY3855 batch 480483 have failed to meet the quoted performance claims prior to expiry on 28th Sept 2020.
Timeline
- Cleared FDA 510(k) K953211
- Listed FDA GUDID 05055273200652
- Recall initiated FDA recalls Z-2923-2020
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Amy
- Generic name
- Alpha-amylase isoenzyme IVD, reagent
- Model / Ref / Catalog
- AY7932
- Primary DI / UDI-DI
- 05055273200652
- 510(k) Number
- FDA product code
- CIJ
- GMDN term
- Alpha-amylase isoenzyme IVD, reagent
- Device class
- Class II
- Regulation number
- 862.1070
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code CIJ (Saccharogenic, Amylase).
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- DART ALPHA-AMYLASE REAGENT SYSTEM by Coulter Electronics, Inc.
- CHEM-STRATE AMYLASE by General Diagnostics
- AMYLASE by Ac Biochemicals, Inc.
- DMA Amylase (Demand) Procedure by Data Medical Associates, Inc.