FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AVL OMNI ANALYZER
K Number: K972733
·
Decision Sep 9, 1997
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
400
Applicant Total
33
Review Days
50
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Basic Information
- Device Name
- AVL OMNI ANALYZER
- K Number
- K972733
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1345
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Avl Scientific Corp.
- Date Received
- July 21, 1997
- Decision Date
- September 9, 1997
- Product Code
- CGA
- 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 |
|---|---|---|---|
| CGA | Glucose Oxidase, Glucose | FDA class 2 | Clinical Chemistry |
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|---|---|---|---|
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| K990092 | AVL OMNI MODULAR ANALYZER | Jan 29, 1999 | Substantially Equivalent |
| K984299 | AVL OPTI CRITICAL CARE ANALYZER | Dec 11, 1998 | Substantially Equivalent |
| K974784 | AVL OPTI CRITICAL CARE ANALYZER | Feb 24, 1998 | Substantially Equivalent |
| K974822 | AVL OPTI-CHECK PH/ BLOOD GAS/ ELECTROLYTE/THB/ SO2 CONTROL | Jan 22, 1998 | Substantially Equivalent |
| K972673 | AVL 9181 ELECTROLYTE ANALYZER | Aug 20, 1997 | Substantially Equivalent |
| K963964 | AVL COMPACT 3 PH/BLOOD GAS ANALYZER | Nov 29, 1996 | Substantially Equivalent |
| K961458 | AVL 9180 ELECTROLYTE ANALYZER | Jun 12, 1996 | Substantially Equivalent |