Alp(Alkaline)(Phosphatase) Reagent
FDA 510(k) K851998 · Alpkem Corp.
510(k) numberK851998
Submission
- Device name
- Alp(Alkaline)(Phosphatase) Reagent
- Applicant
- Alpkem Corp.
Clackamas, OR, US - Received
- May 7, 1985
- Decision date
- May 30, 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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| K890337 | Triglycerides - Gpo ReagentCDT · Traditional | 03/09/1989SE |
| K890336 | Glucose (God) ReagentCGA · Traditional | 02/27/1989SE |
| K890335 | Sodium Hydroxide Solution, Creatinine Reag./Dilu.CGE · Traditional | 02/17/1989SE |
| K890333 | Albumin ReagentEIX · Traditional | 02/17/1989SE |
| K890332 | RFA/2 Rapid Flow Analyzer W/ComputerJJC · Traditional | 02/17/1989SE |
| K883020 | RFA-300 Rapid Flow Analyzer W/ComputerJJF · Traditional | 09/02/1988SE |
| K860367 | Magnesium (Substrate, Enzyme, Reagent)JGF · Traditional | 04/11/1986SE |
Questions and answers
When was Alp(Alkaline)(Phosphatase) Reagent cleared by the FDA?
Alp(Alkaline)(Phosphatase) Reagent (K851998) received a 510(k) decision of Substantially Equivalent on May 30, 1985, 23 days after the submission was received.
What is the product code of K851998?
The FDA product code is CJE – Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes, a Class II (moderate risk) device regulated under 21 CFR 862.1050.