FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SYSMEX QUICKLYSER-II (QLS-200A)
K Number: K882267
·
Decision Jul 12, 1988
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
37
Applicant Total
33
Review Days
42
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Basic Information
- Device Name
- SYSMEX QUICKLYSER-II (QLS-200A)
- K Number
- K882267
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 864.8200
- Medical Specialty
- Hematology
- Decision
- Substantially Equivalent
- Applicant
- Toa Medical Electronics USA, Inc.
- Date Received
- May 31, 1988
- Decision Date
- July 12, 1988
- Product Code
- GIF
- Advisory Committee
- Hematology
- Review Advisory Committee
- HE
- 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 |
|---|---|---|---|
| GIF | Diluent, Blood Cell | FDA class 1 | Hematology |
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Other Clearances by Toa Medical Electronics USA, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K936023 | SYSMEX SE-9000 AUTOMATED HEMATOLOGY ANALYZER | May 2, 1994 | Substantially Equivalent |
| K933886 | TOA MEDICAL ELECTRONICS CA-5000 | Jan 27, 1994 | Substantially Equivalent |
| K931149 | CA-1000 AUTOMATED COAGULATION ANALYZER | Nov 3, 1993 | Substantially Equivalent |
| K920544 | SYSMEX HEMATOLOGY SYSTEM ACCESSORIES | Apr 29, 1992 | Substantially Equivalent |
| K914744 | SYSMEX NE-1500, MODIFICATION | Dec 30, 1991 | Substantially Equivalent |
| K912494 | SYSMEX(TM) R-3000 AUTOMATED RETICULOCYTE ANALYZER | Sep 10, 1991 | Substantially Equivalent |
| K911172 | SYSMEX F-610 | Jul 26, 1991 | Substantially Equivalent |
| K911173 | SYSMEX F-310 | Jul 26, 1991 | Substantially Equivalent |
| K910849 | SYSMEX F-810 | Jul 26, 1991 | Substantially Equivalent |
| K910745 | HEMOGLOBIN REAGENT | Jul 11, 1991 | Substantially Equivalent |