Napa Eia Assay
FDA 510(k) K983812 · Diagnostic Reagents, Inc.
510(k) numberK983812
Submission
- Device name
- Napa Eia Assay
- Applicant
- Diagnostic Reagents, Inc.
Sunnyvale, CA, US - Received
- October 28, 1998
- Decision date
- November 16, 1998
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- LAN – Enzyme Immunoassay, N-Acetylprocainamide
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.3320
- Specialty
- Clinical Toxicology
Other 510(k)s with product code LAN
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K060738 | TDM N-AcetylprocainamideLAN · Traditional | Roche Diagnostics Corp. | 08/16/2006SE |
| K032564 | Dimension N-Acetylprocainamide (Napa) Flex Reagent Cartridge Method, Model DF111LAN · Traditional | Dade Behring, Inc. | 10/31/2003SE |
| K011620 | Emit 2000 N-Acetylprocainamide Assay, Model OSR4N229LAN · Special | Syva Co., Dade Behring, Inc. | 06/18/2001SE |
| K971713 | N-Acetylprocainamide Assay for the Bayer Immuno 1 SystemLAN · Traditional | Bayer Corp. | 06/11/1997SE |
| K955422 | Axsym N-AcetylprocainamideLAN · Traditional | Abbott Laboratories | 04/24/1996SE |
| K934705 | Opus NapaLAN · Traditional | Pb Diagnostic Systems, Inc. | 11/22/1993SE |
| K922915 | Emit 2000 N-Acetylprocainamide Assay and CalibratLAN · Traditional | Syva Co. | 08/24/1992SE |
| K895571 | N-Acetylprocainamide (Napa) (Fpia) KitLAN · Traditional | Tudor Laboratories, Inc. | 10/25/1989SE |
| K873349 | Easy-Test Emit N-Acetylprocainamide Napa #16649LAN · Traditional | Em Diagnostic Systems, Inc. | 09/22/1987SE |
| K871680 | Modified Cobas FP Reagents for Napa and CalibratorLAN · Traditional | Roche Diagnostic Systems, Inc. | 06/08/1987SE |
More from Roche Diagnostic Systems, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K983268 | Modification of Tricyclic Serum Tox Eia AssayLFH · Traditional | 11/18/1998SE |
| K983323 | Digoxin ImmunoassayKXT · Traditional | 11/12/1998SE |
| K983280 | Vancomycin Eia AssayLEH · Traditional | 11/06/1998SE |
| K983159 | Drugs of Abuse Urine Calibrators and ControlsDKB · Traditional | 11/05/1998SE |
| K973102 | Lidocaine Eia AssayKLR · Traditional | 09/12/1997SE |
| K972835 | 50NG/ML Cocaine Metabolite CalibratorDLJ · Traditional | 08/28/1997SE |
| K972526 | Methadone Eia AssayDJR · Traditional | 08/04/1997SE |
| K964212 | Quinidine Enzyme ImmunoassayLBZ · Traditional | 12/18/1996SE |
| K963835 | Digoxin Enzyme ImmunoassayKXT · Traditional | 12/10/1996SE |
| K962463 | Procainamide Enzyme ImmunoassayLAR · Traditional | 08/14/1996SE |
Questions and answers
When was Napa Eia Assay cleared by the FDA?
Napa Eia Assay (K983812) received a 510(k) decision of Substantially Equivalent on November 16, 1998, 19 days after the submission was received.
What is the product code of K983812?
The FDA product code is LAN – Enzyme Immunoassay, N-Acetylprocainamide, a Class II (moderate risk) device regulated under 21 CFR 862.3320.