Select Brand One Step Pregnancy Test
by L. & R. Distributors, Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00015127007269 | Date16 Nov 2016 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- Select Brand
- Generic Name
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
- Model / Reference
- One Step Pregnancy Test
- Primary DI / UDI-DI
- 00015127007269
- 510(k) Number
- FDA Product Code
- LCX
- GMDN Term
- Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
- Device Class
- Class II
- Regulation Number
- 862.1155
- Commercial Distribution
- Not in Commercial Distribution
Other devices from L. & R. Distributors, Inc.
Properties
Other properties (10)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No