Pregnacol Pregnancy Test
FDA 510(k) K972606 · Immunostics Inc.,
510(k) numberK972606
Submission
- Device name
- Pregnacol Pregnancy Test
- Applicant
- Immunostics Inc.,
Ocean, NJ, US - Received
- July 11, 1997
- Decision date
- August 29, 1997
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- JHJ – Agglutination Method, Human Chorionic Gonadotropin
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1155
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JHJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K921968 | In Vitro Diagnostic Reagent Set, Indir. Preg. TestJHJ · Traditional | Tech-Co, Inc. | 06/28/1996SE |
| K935863 | Sas(Tm) Direct Monoclonal HCGJHJ · Traditional | Sa Scientific, Inc. | 02/24/1994SE |
| K926112 | Accutex Beta-Hcg TestJHJ · Traditional | J.S. Medical Assoc. | 07/28/1993SE |
| K930609 | Sas(Tm) Monoclonal Hcg-SlideJHJ · Traditional | Sa Scientific, Inc. | 03/29/1993SE |
| K920716 | Direct Pregnancy TestJHJ · Traditional | Tech-Co, Inc. | 03/24/1992SE |
| K910946 | Clearview HCGJHJ · Traditional | Unipath , Ltd. | 04/01/1991SE |
| K881435 | Pregnospia IIJHJ · Traditional | Organon Teknika Corp. | 05/27/1988SE |
| K880163 | Pregnancy (HCG) Card & Liquid TestJHJ · Traditional | Ampcor, Inc. | 05/17/1988SE |
| K880478 | Pregnancy Beta-Hcg Card & Liquid TestJHJ · Traditional | Ampcor, Inc. | 04/28/1988SE |
| K880328 | Hcg-NostickJHJ · Traditional | Organon Teknika Corp. | 03/15/1988SE |
More from Organon Teknika Corp.
| 510(k) | Device | Decision |
|---|---|---|
| K221817 | ALFIS Vitamin D, ALFIS-3 AnalyzerMRG · Traditional | 09/22/2023SE |
| K182298 | hemochroma PLUS SystemGKR · Traditional | 11/16/2018SE |
| K163465 | hemochroma PLUS SystemGKR · Traditional | 09/08/2017SE |
| K163225 | AFIAS iFOB with AFIAS-50OOX · Traditional | 08/08/2017SE |
| K171484 | hema-screen SPECIFIC GoldKHE · Special | 06/14/2017SE |
| K163554 | hema-screen ER XCEL Enhanced Readability Fecal Occult Blood TestKHE · Special | 01/17/2017SE |
| K102664 | Hema Screen ErKHE · Special | 01/28/2011SE |
| K060463 | Hema Screen Specific IfobtKHE · Traditional | 06/06/2006SE |
| K041728 | HCG Detector Combi, HCG Detector Stix, HCG Detector CassetteJHI · Traditional | 08/11/2004SE |
| K031490 | RubellacolLQN · Traditional | 07/16/2003SE |
Questions and answers
When was Pregnacol Pregnancy Test cleared by the FDA?
Pregnacol Pregnancy Test (K972606) received a 510(k) decision of Substantially Equivalent on August 29, 1997, 49 days after the submission was received.
What is the product code of K972606?
The FDA product code is JHJ – Agglutination Method, Human Chorionic Gonadotropin, a Class II (moderate risk) device regulated under 21 CFR 862.1155.