FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IQ LDH
K Number: K894578
·
Decision Oct 17, 1989
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
12
Applicant Total
632
Review Days
85
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Basic Information
- Device Name
- IQ LDH
- K Number
- K894578
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1440
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Date Received
- July 24, 1989
- Decision Date
- October 17, 1989
- Product Code
- CFH
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- TX
- 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 |
|---|---|---|---|
| CFH | Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (CFH), ordered by most recent decision date.
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LACTATE DEHYDROGENASE (LDH) REAGENT SET
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EDC/TITAN GELISO-DOT TOTAL LDH ISOENZYME PROCEDURE
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·Clinical Chemistry
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