Alkaline Phosphatase
FDA 510(k) K852784 · Advanced Biomedical Methods, Inc.
510(k) numberK852784
Submission
- Device name
- Alkaline Phosphatase
- Applicant
- Advanced Biomedical Methods, Inc.
Niles, IL, US - Received
- July 1, 1985
- Decision date
- July 22, 1985
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- CJE – Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 862.1050
- Specialty
- Clinical Chemistry
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| K240468 | Alkaline PhosphataseCJE · Special | Abbott Laboratories Diagnostics Division | 10/16/2024SE |
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| K171080 | ALP IFCC Gen.2CJE · Special | Roche Diagnostics Operations (Rdo) | 05/10/2017SE |
| K162275 | Randox RX Daytona Plus Alkaline Phosphatase (ALP)CJE · Traditional | Randox Laboratories Limited | 04/21/2017SE |
| K131351 | Ace Alkaline Phosphatase Reagent, Amylase Reagent, Alt Reagent, Ast ReagentCJE · Traditional | Alfa Wassermann Diagnostic Technologies, LLC | 08/15/2013SE |
| K130141 | S Test Reagent Cartridge Alp (Alkaline Phosphatase)CJE · Traditional | Hitachi Chemical Diagnostics, Inc. | 03/22/2013SE |
| K113436 | Ace Alkaline Phosphatase Reagent, Ace Amylase Reagent, Ace Ldh-L ReagentCJE · Traditional | Alfa Wassermann | 07/12/2012SE |
More from Alfa Wassermann
| 510(k) | Device | Decision |
|---|---|---|
| K945353 | Clarit(Tm)JKA · Traditional | 12/09/1994SE |
| K880949 | Single Reagent Calcium for Demand AnalyzerCJY · Traditional | 04/05/1988SE |
| K864866 | Resubmission of the Kleerzit ReagentJKA · Traditional | 03/16/1987SE |
| K852783 | Sgot/Alt ReagentCIT · Traditional | 07/22/1985SE |
| K852027 | GGTP Reagent/Serum Iron/Salicylate Demand AnalyzerDKJ · Traditional | 05/29/1985SE |
| K850381 | Magnesium Reagent for Demand AnalyzerJGJ · Traditional | 03/01/1985SE |
| K850380 | Inorganic Phosphorous for Demand AnalyzerCEO · Traditional | 03/01/1985SE |
| K850379 | Direct Bilirubin for Demand AnalyzerCIG · Traditional | 03/01/1985SE |
| K850378 | LDH Reagent for Demand AnalyzerCFJ · Traditional | 03/01/1985SE |
| K844332 | Creatinine Reagent for Demand AnalyzerCGX · Traditional | 01/03/1985SE |
Questions and answers
When was Alkaline Phosphatase cleared by the FDA?
Alkaline Phosphatase (K852784) received a 510(k) decision of Substantially Equivalent on July 22, 1985, 21 days after the submission was received.
What is the product code of K852784?
The FDA product code is CJE – Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1050.