FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
STRATUS(R) CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
K Number: K900806
·
Decision Mar 23, 1990
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
37
Applicant Total
505
Review Days
30
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Basic Information
- Device Name
- STRATUS(R) CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
- K Number
- K900806
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1215
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Baxter Healthcare Corp
- Date Received
- February 21, 1990
- Decision Date
- March 23, 1990
- Product Code
- JHS
- 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 |
|---|---|---|---|
| JHS | Differential Rate Kinetic Method, Cpk Or Isoenzymes | FDA class 2 | Clinical Chemistry |
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