Delfia(R) 17 -Oh-Progesteron Kit
FDA 510(k) K912026 · Pharmacia Diagnostics, Inc.
510(k) numberK912026
Submission
- Device name
- Delfia(R) 17 -Oh-Progesteron Kit
- Applicant
- Pharmacia Diagnostics, Inc.
Columbia, MD, US - Received
- May 7, 1991
- Decision date
- June 25, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- JLX – Radioimmunoassay, 17-Hydroxyprogesterone
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1395
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JLX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K100682 | GSP Neonatal 17A-OH-PROGESTERONE Kit Model: 3305-001UJLX · Traditional | Wallac OY | 07/23/2010SE |
| K081922 | Autodelfia Neonatal 17A-OH-PROGESTERONE KitJLX · Traditional | Wallac OY | 04/16/2009SE |
| K062534 | Enzyme Immunoassay for the Detection of Salivary 17-A-HYDROXYPROGESTERONEJLX · Traditional | Drg Intl., Inc. | 01/29/2008SE |
| K060452 | Accuwell 17-ALPHA-HYDROXYPROESTERONE Enzyme Immunoassay with Models 6015XX-ECAHJLX · Abbreviated | Neo-Genesis | 03/13/2007SE |
| K050960 | Modification to: Autodelfia Neonatal 17A-OH-PROGESTERONE L KitJLX · Special | Wallac OY | 07/11/2005SE |
| K042425 | Autodelfia Neonatal 17A-OH-PROGESTERONE KitJLX · Special | Wallac OY | 09/30/2004SE |
| K042424 | Delfia Neonatal 17A-OH-PROGESTERONE KitJLX · Special | Wallac OY | 09/30/2004SE |
| K973350 | Bio-Rad Microplate 17-HYDROXYPROGESTERONE TestJLX · Traditional | Bio-Rad | 02/09/1998SE |
| K934178 | Accuscreen 17-HYDROXYPROGESTERONEJLX · Traditional | Neometrics, Inc. | 03/30/1995SE |
| K940233 | Neoscreen Elisa HydroxyprogesteroneJLX · Traditional | Pantex | 12/28/1994SE |
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Questions and answers
When was Delfia(R) 17 -Oh-Progesteron Kit cleared by the FDA?
Delfia(R) 17 -Oh-Progesteron Kit (K912026) received a 510(k) decision of Substantially Equivalent on June 25, 1991, 49 days after the submission was received.
What is the product code of K912026?
The FDA product code is JLX – Radioimmunoassay, 17-Hydroxyprogesterone, a Class I (low risk) device regulated under 21 CFR 862.1395.