FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
FETAL-TEK CONTROL (IMMATURE/BORDERLINE)
K Number: K820772
·
Decision May 12, 1982
Classifications
1
FEI Numbers
280
Registration Numbers
280
Same Product Code
492
Applicant Total
280
Review Days
50
Basic Information
- Device Name
- FETAL-TEK CONTROL (IMMATURE/BORDERLINE)
- K Number
- K820772
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- HELENA LABORATORIES
- Date Received
- March 23, 1982
- Decision Date
- May 12, 1982
- Product Code
- JJX
- 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 |
|---|---|---|---|
| JJX | Single (Specified) Analyte Controls (Assayed And Unassayed) | FDA class 1 | Clinical Chemistry |
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