FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TESTPACK ACUTE HCG SERUM CONTROLS
K Number: K863126
·
Decision Sep 15, 1986
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
883
Review Days
31
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Basic Information
- Device Name
- TESTPACK ACUTE HCG SERUM CONTROLS
- K Number
- K863126
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.1660
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- August 15, 1986
- Decision Date
- September 15, 1986
- 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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