Precise TM HCG
FDA 510(k) K915197 · Becton Dickinson Advanced Diagnostics
510(k) numberK915197
Submission
- Device name
- Precise TM HCG
- Applicant
- Becton Dickinson Advanced Diagnostics
Cockeysville, MD, US - Received
- November 19, 1991
- Decision date
- December 17, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- JHI – Visual, Pregnancy Hcg, Prescription Use
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1155
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JHI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K241919 | Innovita HCG Pregnancy Rapid Combo TestJHI · Traditional | Innovita (Tangshan) Biological Technology Co.… | 08/02/2024SE |
| K203272 | Alltest Pregnancy Rapid Combo Test CassetteJHI · Traditional | Hangzhou AllTest Biotech Co., Ltd. | 01/31/2022SE |
| K172322 | Atellica IM Total hCG (ThCG)JHI · Traditional | Siemens Healthcare Diagnostics, Inc. | 03/29/2018SE |
| K172257 | TrueDX hCG Early Result Pregnancy Test (Midstream Format), TrueDX hCG Early Result…JHI · Traditional | True Diagnostics, Inc. | 12/22/2017SE |
| K152768 | Assure Tech hCG Pregnancy Serum/Urine Combo Test Cassette, Assure Tech hCG Pregnancy…JHI · Traditional | Assure Tech. Co., Ltd. | 02/24/2016SE |
| K130456 | Wunder Pregnancy TestJHI · Traditional | James Nguyen | 04/08/2014SE |
| K132834 | Fastep S10 HCG Serum/Urine Combo TestJHI · Traditional | Polymed Therapeutics, Inc. | 01/09/2014SE |
| K131166 | Sofia(R) HCG FiaJHI · Traditional | Quidel Corp. | 08/02/2013SE |
| K123844 | Chemtrue HCG Pregnancy Urine Dipstick, HCG Pregnancy Urine Cassette Test, and HCG Combo…JHI · Traditional | Chemtron Biotech, Inc. | 05/30/2013SE |
| K112101 | Fastep HCG Pregancy Serum/Urine Cassette and Dipstick TestsJHI · Traditional | Polymed Therapeutics, Inc. | 07/17/2012SE |
More from Polymed Therapeutics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K935667 | Qtest(R) StrepGTY · Traditional | 04/21/1994SE |
| K931294 | Iq Tuptake AssayKHQ · Traditional | 07/22/1993SE |
| K931295 | Iq TT4 AssayCDX · Traditional | 07/20/1993SE |
| K926356 | Precise(Tm) Hcg(Urine/Serum) and Prcise(Tm) PregJHI · Traditional | 03/18/1993SE |
| K925132 | Becton Dickinson Thyroid Stimulating Hormone SysteJLW · Traditional | 12/28/1992SE |
| K923673 | Precise Strep aGTZ · Traditional | 09/28/1992SE |
| K923060 | Iq Immunochemistry Sistem; Iq TSH AssayJJE · Traditional | 09/15/1992SE |
| K914958 | Riatrac PlusJJY · Traditional | 03/18/1992SE |
| K915200 | Precise TM HCG for Use in the Physicians Office laJHI · Traditional | 12/16/1991SE |
Questions and answers
When was Precise TM HCG cleared by the FDA?
Precise TM HCG (K915197) received a 510(k) decision of Substantially Equivalent on December 17, 1991, 28 days after the submission was received.
What is the product code of K915197?
The FDA product code is JHI – Visual, Pregnancy Hcg, Prescription Use, a Class II (moderate risk) device regulated under 21 CFR 862.1155.