FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CHLORIDE REAGENT KIT
K Number: K811319
·
Decision Aug 13, 1981
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
18
Applicant Total
9
Review Days
93
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Basic Information
- Device Name
- CHLORIDE REAGENT KIT
- K Number
- K811319
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1170
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Chem-Elec, Inc.
- Date Received
- May 12, 1981
- Decision Date
- August 13, 1981
- Product Code
- JFS
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JFS | Coulometric, Chloride | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JFS), ordered by most recent decision date.
CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRIC
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REAGENTS CORNING CHLORIDE METER FOR
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RERMCO TEST CHLORIDE REAGENT
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LIQUIZYME CHLORIDE REAGENT
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Other Clearances by Chem-Elec, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K943503 | CHEMCARD GLUCOSE TEST | Jul 23, 1996 | Substantially Equivalent |
| K864159 | SOLID PHASE DETER SERUM CHOLESTEROL FR WHOLE BLOOD | Jun 10, 1988 | Substantially Equivalent |
| K811165 | GLUCOSE OXIDASE RATE REAGENT | Aug 13, 1981 | Substantially Equivalent |
| K811406 | CREATININE RATE REAGENT KIT | Aug 13, 1981 | Substantially Equivalent |
| K811381 | ASTRA | Aug 13, 1981 | Substantially Equivalent |
| K811193 | BUN RATE REAGENT | Jul 10, 1981 | Substantially Equivalent |
| K811310 | SODIUM/POTASSIUM REAGENT KITS | Jul 10, 1981 | Substantially Equivalent |
| K811701 | CHLORIDE/CARBON DIOXIDE RATE REAGENT | Jul 1, 1981 | Substantially Equivalent |